FDA Approved Products

Application #	Type	Sponsor	Product #	Drug Name	Form	Strength	Active Ingredient	Approval Date	Marketing Status	Reference Standard
220073	NDA	BRISTOL	002	ELIQUIS	TABLET;ORAL	5MG	APIXABAN	2025-04-17	Prescription	No
			003	ELIQUIS	TABLET;ORAL	0.5MG	APIXABAN	2025-04-17	Prescription	No
			004	ELIQUIS	SUSPENSION;ORAL	0.15MG	APIXABAN	2025-04-17	Prescription	No
			001	ELIQUIS SPRINKLE	FOR SUSPENSION;ORAL	0.15MG	APIXABAN	2025-04-17	Prescription	Yes
761381	BLA	BRISTOL-MYERS SQUIBB	001	OPDIVO QVANTIG	INJECTABLE;SUBCUTANEOUS	600MG;10000UNITS PER5ML(120MG/2000UNITS PER ML)	NIVOLUMAB;HYALURONIDASE-NVHY	2024-12-27	Prescription	No
761429	BLA	BRISTOL-MYERS SQUIBB	001	OPDIVO QVANTIG	INJECTABLE;INJECTION	600MG;10000 UNITS PER 5ML(120MG/2000UNITS PER ML)	NIVOLUMAB;HYALURONIDASE-NVHY	2024-12-27	Prescription	No
216158	NDA	BRISTOL-MYERS	001	COBENFY	CAPSULE;ORAL	20MG;EQ 50MG BASE	TROSPIUM CHLORIDE; XANOMELINE TARTRATE	2024-09-26	Prescription	No
			002	COBENFY	CAPSULE;ORAL	20MG;EQ 100MG BASE	TROSPIUM CHLORIDE; XANOMELINE TARTRATE	2024-09-26	Prescription	No
			003	COBENFY	CAPSULE;ORAL	30MG;EQ 125MG BASE	TROSPIUM CHLORIDE; XANOMELINE TARTRATE	2024-09-26	Prescription	Yes
218213	NDA	BRISTOL	001	AUGTYRO	CAPSULE;ORAL	40MG	REPOTRECTINIB	2023-11-15	Prescription	Yes
218213	NDA	BRISTOL	002	AUGTYRO	CAPSULE;ORAL	160MG	REPOTRECTINIB	2023-11-15	Prescription	Yes
216340	NDA	BRISTOL	001	KRAZATI	TABLET;ORAL	200MG	ADAGRASIB	2022-12-12	Prescription	Yes
214958	NDA	BRISTOL	001	SOTYKTU	TABLET;ORAL	6MG	DEUCRAVACITINIB	2022-09-09	Prescription	Yes
214998	NDA	BRISTOL	001	CAMZYOS	CAPSULE;ORAL	2.5MG	MAVACAMTEN	2022-04-28	Prescription	No
			002	CAMZYOS	CAPSULE;ORAL	5MG	MAVACAMTEN	2022-04-28	Prescription	Yes
			003	CAMZYOS	CAPSULE;ORAL	10MG	MAVACAMTEN	2022-04-28	Prescription	No
			004	CAMZYOS	CAPSULE;ORAL	15MG	MAVACAMTEN	2022-04-28	Prescription	No
761234	BLA	BRISTOL MYERS SQUIBB	001	OPDUALAG	SOLUTION;INTRAVENOUS	240MG;80MG	NIVOLUMAB;RELATLIMAB-RMBW	2022-03-18	Prescription	No
214120	NDA	BRISTOL	001	ONUREG	TABLET;ORAL	200MG	AZACITIDINE	2020-09-01	Prescription	No
214120	NDA	BRISTOL	002	ONUREG	TABLET;ORAL	300MG	AZACITIDINE	2020-09-01	Prescription	Yes
209899	NDA	BRISTOL	001	ZEPOSIA	CAPSULE;ORAL	EQ 0.23MG BASE	OZANIMOD HYDROCHLORIDE	2020-03-25	Prescription	No
			002	ZEPOSIA	CAPSULE;ORAL	EQ 0.46MG BASE	OZANIMOD HYDROCHLORIDE	2020-03-25	Prescription	No
			003	ZEPOSIA	CAPSULE;ORAL	EQ 0.92MG BASE	OZANIMOD HYDROCHLORIDE	2020-03-25	Prescription	Yes
212327	NDA	BRISTOL-MYERS	001	INREBIC	CAPSULE;ORAL	EQ 100MG BASE	FEDRATINIB HYDROCHLORIDE	2019-08-16	Prescription	Yes
209606	NDA	BRISTOL MYERS SQUIBB	001	IDHIFA	TABLET;ORAL	EQ 50MG BASE	ENASIDENIB MESYLATE	2017-08-01	Prescription	No
209606	NDA	BRISTOL MYERS SQUIBB	002	IDHIFA	TABLET;ORAL	EQ 100MG BASE	ENASIDENIB MESYLATE	2017-08-01	Prescription	Yes
761035	BLA	BRISTOL MYERS SQUIBB	001	EMPLICITI	INJECTABLE;INJECTION	300MG	ELOTUZUMAB	2015-11-30	Prescription	No
761035	BLA	BRISTOL MYERS SQUIBB	002	EMPLICITI	INJECTABLE;INJECTION	400MG	ELOTUZUMAB	2015-11-30	Prescription	No
206843	NDA	BRISTOL-MYERS SQUIBB	001	DAKLINZA	TABLET;ORAL	EQ 30MG BASE	DACLATASVIR DIHYDROCHLORIDE	2015-07-24	Discontinued	No
			002	DAKLINZA	TABLET;ORAL	EQ 60MG BASE	DACLATASVIR DIHYDROCHLORIDE	2015-07-24	Discontinued	No
			003	DAKLINZA	TABLET;ORAL	EQ 90MG BASE	DACLATASVIR DIHYDROCHLORIDE	2015-07-24	Discontinued	No
125527	BLA	BRISTOL MYERS SQUIBB	001	OPDIVO	INJECTABLE;INJECTION	40MG/4ML	NIVOLUMAB	2015-03-04	Prescription	No
125527	BLA	BRISTOL MYERS SQUIBB	002	OPDIVO	INJECTABLE;INJECTION	100MG/10ML	NIVOLUMAB	2015-03-04	Prescription	No
206353	NDA	BRISTOL	001	EVOTAZ	TABLET;ORAL	EQ 300MG BASE;150MG	ATAZANAVIR SULFATE; COBICISTAT	2015-01-29	Prescription	Yes
125554	BLA	BRISTOL MYERS SQUIBB	001	OPDIVO	INJECTABLE;INJECTION	40MG/4ML	NIVOLUMAB	2014-12-22	Prescription	No
206352	NDA	BRISTOL MYERS SQUIBB	001	REYATAZ	POWDER;ORAL	EQ 50MG BASE/PACKET	ATAZANAVIR SULFATE	2014-06-02	Prescription	Yes
204026	NDA	BRISTOL	001	POMALYST	CAPSULE;ORAL	1MG	POMALIDOMIDE	2013-02-08	Prescription	No
			002	POMALYST	CAPSULE;ORAL	2MG	POMALIDOMIDE	2013-02-08	Prescription	No
			003	POMALYST	CAPSULE;ORAL	3MG	POMALIDOMIDE	2013-02-08	Prescription	No
			004	POMALYST	CAPSULE;ORAL	4MG	POMALIDOMIDE	2013-02-08	Prescription	Yes
202155	NDA	BRISTOL MYERS SQUIBB	001	ELIQUIS	TABLET;ORAL	2.5MG	APIXABAN	2012-12-28	Prescription	No
			002	ELIQUIS	TABLET;ORAL	5MG	APIXABAN	2012-12-28	Prescription	Yes
			003	ELIQUIS	TABLET, FOR SUSPENSION;ORAL	0.5MG	APIXABAN	2012-12-28	Prescription	Yes
125288	BLA	BRISTOL MYERS SQUIBB	001	NULOJIX	INJECTABLE; INJECTION	250MG	BELATACEPT	2011-06-15	Prescription	No
125377	BLA	BRISTOL MYERS SQUIBB	001	YERVOY	INJECTABLE; INJECTION	3MG	IPILIMUMAB	2011-03-25	Prescription	No
022393	NDA	BRISTOL-MYERS	001	ISTODAX	POWDER;INTRAVENOUS	10MG/VIAL	ROMIDEPSIN	2009-11-05	Prescription	Yes
021986	NDA	BRISTOL MYERS SQUIBB	001	SPRYCEL	TABLET;ORAL	20MG	DASATINIB	2006-06-28	Prescription	No
			002	SPRYCEL	TABLET;ORAL	50MG	DASATINIB	2006-06-28	Prescription	No
			003	SPRYCEL	TABLET;ORAL	70MG	DASATINIB	2006-06-28	Prescription	No
			004	SPRYCEL	TABLET;ORAL	100MG	DASATINIB	2006-06-28	Prescription	Yes
			005	SPRYCEL	TABLET;ORAL	80MG	DASATINIB	2006-06-28	Prescription	No
			006	SPRYCEL	TABLET;ORAL	140MG	DASATINIB	2006-06-28	Prescription	No
022072	NDA	BRISTOL MYERS SQUIBB	001	SPRYCEL	TABLET; ORAL	70MG	DASATINIB	2006-06-28	Prescription	No
021880	NDA	BRISTOL MYERS SQUIBB	001	REVLIMID	CAPSULE;ORAL	5MG	LENALIDOMIDE	2005-12-27	Prescription	No
			002	REVLIMID	CAPSULE;ORAL	10MG	LENALIDOMIDE	2005-12-27	Prescription	No
			003	REVLIMID	CAPSULE;ORAL	15MG	LENALIDOMIDE	2005-12-27	Prescription	No
			004	REVLIMID	CAPSULE;ORAL	25MG	LENALIDOMIDE	2005-12-27	Prescription	Yes
			005	REVLIMID	CAPSULE;ORAL	2.5MG	LENALIDOMIDE	2005-12-27	Prescription	No
			006	REVLIMID	CAPSULE;ORAL	20MG	LENALIDOMIDE	2005-12-27	Prescription	No
125118	BLA	BRISTOL MYERS SQUIBB	001	ORENCIA	INJECTABLE; IV (INFUSION)	250MG	ABATACEPT	2005-12-23	Prescription	No
021797	NDA	BRISTOL MYERS SQUIBB	001	BARACLUDE	TABLET;ORAL	0.5MG	ENTECAVIR	2005-03-29	Prescription	No
021797	NDA	BRISTOL MYERS SQUIBB	002	BARACLUDE	TABLET;ORAL	1MG	ENTECAVIR	2005-03-29	Prescription	Yes
021798	NDA	BRISTOL MYERS SQUIBB	001	BARACLUDE	SOLUTION;ORAL	0.05MG/ML	ENTECAVIR	2005-03-29	Prescription	Yes
021660	NDA	BRISTOL-MYERS	001	ABRAXANE	POWDER;INTRAVENOUS	100MG/VIAL	PACLITAXEL	2005-01-07	Prescription	Yes
050794	NDA	BRISTOL-MYERS	001	VIDAZA	POWDER;INTRAVENOUS, SUBCUTANEOUS	100MG/VIAL	AZACITIDINE	2004-05-19	Prescription	Yes
021387	NDA	BRISTOL MYERS SQUIBB	001	PRAVIGARD PAC (COPACKAGED)	TABLET;ORAL	81MG;20MG	ASPIRIN; PRAVASTATIN SODIUM	2003-06-24	Discontinued	No
			002	PRAVIGARD PAC (COPACKAGED)	TABLET;ORAL	81MG;40MG	ASPIRIN; PRAVASTATIN SODIUM	2003-06-24	Discontinued	No
			003	PRAVIGARD PAC (COPACKAGED)	TABLET;ORAL	81MG;80MG	ASPIRIN; PRAVASTATIN SODIUM	2003-06-24	Discontinued	No
			004	PRAVIGARD PAC (COPACKAGED)	TABLET;ORAL	325MG;20MG	ASPIRIN; PRAVASTATIN SODIUM	2003-06-24	Discontinued	No
			005	PRAVIGARD PAC (COPACKAGED)	TABLET;ORAL	325MG;40MG	ASPIRIN; PRAVASTATIN SODIUM	2003-06-24	Discontinued	No
			006	PRAVIGARD PAC (COPACKAGED)	TABLET;ORAL	325MG;80MG	ASPIRIN; PRAVASTATIN SODIUM	2003-06-24	Discontinued	No
021567	NDA	BRISTOL MYERS SQUIBB	001	REYATAZ	CAPSULE;ORAL	EQ 100MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ATAZANAVIR SULFATE	2003-06-20	Discontinued	No
			002	REYATAZ	CAPSULE;ORAL	EQ 150MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ATAZANAVIR SULFATE	2003-06-20	Discontinued	No
			003	REYATAZ	CAPSULE;ORAL	EQ 200MG BASE	ATAZANAVIR SULFATE	2003-06-20	Prescription	No
			004	REYATAZ	CAPSULE;ORAL	EQ 300MG BASE	ATAZANAVIR SULFATE	2003-06-20	Prescription	Yes
021453	NDA	BRISTOL MYERS SQUIBB	001	ZERIT XR	CAPSULE, EXTENDED RELEASE;ORAL	37.5MG	STAVUDINE	2002-12-31	Discontinued	No
			002	ZERIT XR	CAPSULE, EXTENDED RELEASE;ORAL	50MG	STAVUDINE	2002-12-31	Discontinued	No
			003	ZERIT XR	CAPSULE, EXTENDED RELEASE;ORAL	75MG	STAVUDINE	2002-12-31	Discontinued	No
			004	ZERIT XR	CAPSULE, EXTENDED RELEASE;ORAL	100MG	STAVUDINE	2002-12-31	Discontinued	No
021460	NDA	BRISTOL MYERS SQUIBB	001	METAGLIP	TABLET;ORAL	2.5MG;250MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	GLIPIZIDE; METFORMIN HYDROCHLORIDE	2002-10-21	Discontinued	No
			002	METAGLIP	TABLET;ORAL	2.5MG;500MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	GLIPIZIDE; METFORMIN HYDROCHLORIDE	2002-10-21	Discontinued	No
			003	METAGLIP	TABLET;ORAL	5MG;500MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	GLIPIZIDE; METFORMIN HYDROCHLORIDE	2002-10-21	Discontinued	No
021360	NDA	BRISTOL MYERS SQUIBB	001	SUSTIVA	TABLET;ORAL	300MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	EFAVIRENZ	2002-02-01	Discontinued	No
021360	NDA	BRISTOL MYERS SQUIBB	002	SUSTIVA	TABLET;ORAL	600MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	EFAVIRENZ	2002-02-01	Discontinued	No
021190	NDA	BRISTOL MYERS SQUIBB	001	BUSPAR	CAPSULE;ORAL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	BUSPIRONE HYDROCHLORIDE	2000-12-20	Discontinued	No
			002	BUSPAR	CAPSULE;ORAL	7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	BUSPIRONE HYDROCHLORIDE	2000-12-20	Discontinued	No
			003	BUSPAR	CAPSULE;ORAL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	BUSPIRONE HYDROCHLORIDE	2000-12-20	Discontinued	No
			004	BUSPAR	CAPSULE;ORAL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	BUSPIRONE HYDROCHLORIDE	2000-12-20	Discontinued	No
021183	NDA	BRISTOL MYERS SQUIBB	001	VIDEX EC	CAPSULE, DELAYED REL PELLETS;ORAL	125MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DIDANOSINE	2000-10-31	Discontinued	No
			002	VIDEX EC	CAPSULE, DELAYED REL PELLETS;ORAL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DIDANOSINE	2000-10-31	Discontinued	No
			003	VIDEX EC	CAPSULE, DELAYED REL PELLETS;ORAL	250MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DIDANOSINE	2000-10-31	Discontinued	No
			004	VIDEX EC	CAPSULE, DELAYED REL PELLETS;ORAL	400MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DIDANOSINE	2000-10-31	Discontinued	No
021178	NDA	BRISTOL MYERS SQUIBB	001	GLUCOVANCE	TABLET;ORAL	1.25MG;250MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	GLYBURIDE; METFORMIN HYDROCHLORIDE	2000-07-31	Discontinued	No
			002	GLUCOVANCE	TABLET;ORAL	2.5MG;500MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	GLYBURIDE; METFORMIN HYDROCHLORIDE	2000-07-31	Discontinued	No
			003	GLUCOVANCE	TABLET;ORAL	5MG;500MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	GLYBURIDE; METFORMIN HYDROCHLORIDE	2000-07-31	Discontinued	No
020972	NDA	BRISTOL MYERS SQUIBB	001	SUSTIVA	CAPSULE;ORAL	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	EFAVIRENZ	1998-09-17	Discontinued	No
			002	SUSTIVA	CAPSULE;ORAL	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	EFAVIRENZ	1998-09-17	Discontinued	No
			003	SUSTIVA	CAPSULE;ORAL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	EFAVIRENZ	1998-09-17	Discontinued	No
020785	NDA	BRISTOL-MYERS	001	THALOMID	CAPSULE;ORAL	50MG	THALIDOMIDE	1998-07-16	Prescription	No
			002	THALOMID	CAPSULE;ORAL	100MG	THALIDOMIDE	1998-07-16	Prescription	No
			003	THALOMID	CAPSULE;ORAL	200MG	THALIDOMIDE	1998-07-16	Prescription	Yes
			004	THALOMID	CAPSULE;ORAL	150MG	THALIDOMIDE	1998-07-16	Prescription	No
020906	NDA	BRISTOL MYERS SQUIBB	001	ETOPOPHOS PRESERVATIVE FREE	INJECTABLE;INJECTION	EQ 500MG BASE/VIAL	ETOPOSIDE PHOSPHATE	1998-02-27	Discontinued	No
020906	NDA	BRISTOL MYERS SQUIBB	002	ETOPOPHOS PRESERVATIVE FREE	INJECTABLE;INJECTION	EQ 1GM BASE/VIAL	ETOPOSIDE PHOSPHATE	1998-02-27	Discontinued	No
020413	NDA	BRISTOL	001	ZERIT	FOR SOLUTION;ORAL	1MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	STAVUDINE	1996-09-06	Discontinued	No
020152	NDA	BRISTOL MYERS SQUIBB	001	SERZONE	TABLET;ORAL	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	NEFAZODONE HYDROCHLORIDE	1994-12-22	Discontinued	No
			002	SERZONE	TABLET;ORAL	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	NEFAZODONE HYDROCHLORIDE	1994-12-22	Discontinued	No
			003	SERZONE	TABLET;ORAL	150MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	NEFAZODONE HYDROCHLORIDE	1994-12-22	Discontinued	No
			004	SERZONE	TABLET;ORAL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	NEFAZODONE HYDROCHLORIDE	1994-12-22	Discontinued	No
			005	SERZONE	TABLET;ORAL	250MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	NEFAZODONE HYDROCHLORIDE	1994-12-22	Discontinued	No
			006	SERZONE	TABLET;ORAL	300MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	NEFAZODONE HYDROCHLORIDE	1994-12-22	Discontinued	No
020286	NDA	BRISTOL MYERS SQUIBB	001	MONOPRIL-HCT	TABLET;ORAL	20MG;12.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE	1994-11-30	Discontinued	No
020286	NDA	BRISTOL MYERS SQUIBB	002	MONOPRIL-HCT	TABLET;ORAL	10MG;12.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE	1994-11-30	Discontinued	No
020412	NDA	BRISTOL	001	ZERIT	CAPSULE;ORAL	5MG	STAVUDINE	1994-06-24	Discontinued	No
			002	ZERIT	CAPSULE;ORAL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	STAVUDINE	1994-06-24	Discontinued	No
			003	ZERIT	CAPSULE;ORAL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	STAVUDINE	1994-06-24	Discontinued	No
			004	ZERIT	CAPSULE;ORAL	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	STAVUDINE	1994-06-24	Discontinued	No
			005	ZERIT	CAPSULE;ORAL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	STAVUDINE	1994-06-24	Discontinued	No
020264	NDA	BRISTOL MYERS SQUIBB	001	MEGACE	SUSPENSION;ORAL	40MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MEGESTROL ACETATE	1993-09-10	Discontinued	No
081295	ANDA	BRISTOL MYERS SQUIBB	001	ESTRACE	TABLET;ORAL	0.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ESTRADIOL	1993-06-30	Discontinued	No
019890	NDA	BRISTOL MYERS SQUIBB	001	STADOL	SPRAY, METERED;NASAL	1MG/SPRAY Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	BUTORPHANOL TARTRATE	1991-12-12	Discontinued	No
019898	NDA	BRISTOL MYERS SQUIBB	002	PRAVACHOL	TABLET;ORAL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	PRAVASTATIN SODIUM	1991-10-31	Discontinued	No
			003	PRAVACHOL	TABLET;ORAL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	PRAVASTATIN SODIUM	1991-10-31	Discontinued	No
			004	PRAVACHOL	TABLET;ORAL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	PRAVASTATIN SODIUM	1991-10-31	Discontinued	No
			008	PRAVACHOL	TABLET;ORAL	80MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	PRAVASTATIN SODIUM	1991-10-31	Discontinued	No
020156	NDA	BRISTOL	001	VIDEX	FOR SOLUTION;ORAL	10MG/ML	DIDANOSINE	1991-10-09	Discontinued	No
020154	NDA	BRISTOL MYERS SQUIBB	002	VIDEX	TABLET, CHEWABLE;ORAL	25MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DIDANOSINE	1991-10-09	Discontinued	No
			003	VIDEX	TABLET, CHEWABLE;ORAL	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DIDANOSINE	1991-10-09	Discontinued	No
			004	VIDEX	TABLET, CHEWABLE;ORAL	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DIDANOSINE	1991-10-09	Discontinued	No
			005	VIDEX	TABLET, CHEWABLE;ORAL	150MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DIDANOSINE	1991-10-09	Discontinued	No
			006	VIDEX	TABLET, CHEWABLE;ORAL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DIDANOSINE	1991-10-09	Discontinued	No
020155	NDA	BRISTOL MYERS SQUIBB	003	VIDEX	FOR SOLUTION;ORAL	100MG/PACKET	DIDANOSINE	1991-10-09	Discontinued	No
			004	VIDEX	FOR SOLUTION;ORAL	167MG/PACKET	DIDANOSINE	1991-10-09	Discontinued	No
			005	VIDEX	FOR SOLUTION;ORAL	250MG/PACKET	DIDANOSINE	1991-10-09	Discontinued	No
			006	VIDEX	FOR SOLUTION;ORAL	375MG/PACKET	DIDANOSINE	1991-10-09	Discontinued	No
019915	NDA	BRISTOL MYERS SQUIBB	002	MONOPRIL	TABLET;ORAL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	FOSINOPRIL SODIUM	1991-05-16	Discontinued	No
			003	MONOPRIL	TABLET;ORAL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	FOSINOPRIL SODIUM	1991-05-16	Discontinued	No
			004	MONOPRIL	TABLET;ORAL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	FOSINOPRIL SODIUM	1991-05-16	Discontinued	No
050632	NDA	BRISTOL MYERS SQUIBB	001	AZACTAM IN PLASTIC CONTAINER	INJECTABLE;INJECTION	40MG/ML	AZTREONAM	1989-05-24	Discontinued	No
			002	AZACTAM IN PLASTIC CONTAINER	INJECTABLE;INJECTION	20MG/ML	AZTREONAM	1989-05-24	Discontinued	No
			003	AZACTAM IN PLASTIC CONTAINER	INJECTABLE;INJECTION	10MG/ML	AZTREONAM	1989-05-24	Discontinued	No
089887	ANDA	BRISTOL MYERS SQUIBB	001	MEXATE-AQ PRESERVED	INJECTABLE;INJECTION	EQ 25MG BASE/ML	METHOTREXATE SODIUM	1989-04-14	Discontinued	No
062926	ANDA	BRISTOL MYERS SQUIBB	001	RUBEX	INJECTABLE;INJECTION	10MG/VIAL	DOXORUBICIN HYDROCHLORIDE	1989-04-13	Discontinued	No
			002	RUBEX	INJECTABLE;INJECTION	50MG/VIAL	DOXORUBICIN HYDROCHLORIDE	1989-04-13	Discontinued	No
			003	RUBEX	INJECTABLE;INJECTION	100MG/VIAL	DOXORUBICIN HYDROCHLORIDE	1989-04-13	Discontinued	No
019669	NDA	BRISTOL MYERS	001	QUESTRAN LIGHT	POWDER;ORAL	EQ 4GM RESIN/PACKET Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CHOLESTYRAMINE	1988-12-05	Discontinued	No
019669	NDA	BRISTOL MYERS	003	QUESTRAN LIGHT	POWDER;ORAL	EQ 4GM RESIN/SCOOPFUL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CHOLESTYRAMINE	1988-12-05	Discontinued	No
071083	ANDA	BRISTOL MYERS SQUIBB	001	NARCAN	INJECTABLE;INJECTION	0.4MG/ML	NALOXONE HYDROCHLORIDE	1988-07-28	Discontinued	No
071084	ANDA	BRISTOL MYERS SQUIBB	001	NARCAN	INJECTABLE;INJECTION	1MG/ML	NALOXONE HYDROCHLORIDE	1988-07-28	Discontinued	No
071311	ANDA	BRISTOL MYERS SQUIBB	001	NARCAN	INJECTABLE;INJECTION	1MG/ML	NALOXONE HYDROCHLORIDE	1988-07-28	Discontinued	No
070867	ANDA	BRISTOL MYERS SQUIBB	001	VINCREX	INJECTABLE;INJECTION	5MG/VIAL	VINCRISTINE SULFATE	1988-07-12	Discontinued	No
072035	ANDA	BRISTOL MYERS	001	NUPRIN	TABLET;ORAL	200MG	IBUPROFEN	1988-02-16	Discontinued	No
072036	ANDA	BRISTOL MYERS	001	NUPRIN	TABLET;ORAL	200MG	IBUPROFEN	1988-02-16	Discontinued	No
050580	NDA	BRISTOL MYERS SQUIBB	001	AZACTAM	INJECTABLE;INJECTION	500MG/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	AZTREONAM	1986-12-31	Discontinued	No
			002	AZACTAM	INJECTABLE;INJECTION	1GM/VIAL	AZTREONAM	1986-12-31	Prescription	Yes
			003	AZACTAM	INJECTABLE;INJECTION	2GM/VIAL	AZTREONAM	1986-12-31	Prescription	Yes
018731	NDA	BRISTOL MYERS SQUIBB	001	BUSPAR	TABLET;ORAL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	BUSPIRONE HYDROCHLORIDE	1986-09-29	Discontinued	No
			002	BUSPAR	TABLET;ORAL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	BUSPIRONE HYDROCHLORIDE	1986-09-29	Discontinued	No
			003	BUSPAR	TABLET;ORAL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	BUSPIRONE HYDROCHLORIDE	1986-09-29	Discontinued	No
			004	BUSPAR	TABLET;ORAL	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	BUSPIRONE HYDROCHLORIDE	1986-09-29	Discontinued	No
088760	ANDA	BRISTOL MYERS	001	MEXATE-AQ	INJECTABLE;INJECTION	EQ 25MG BASE/ML	METHOTREXATE SODIUM	1985-02-14	Discontinued	No
050554	NDA	BRISTOL	001	PRECEF	INJECTABLE;INJECTION	500MG/VIAL	CEFORANIDE	1984-05-24	Discontinued	No
			002	PRECEF	INJECTABLE;INJECTION	1GM/VIAL	CEFORANIDE	1984-05-24	Discontinued	No
			003	PRECEF	INJECTABLE;INJECTION	2GM/VIAL	CEFORANIDE	1984-05-24	Discontinued	No
			004	PRECEF	INJECTABLE;INJECTION	10GM/VIAL	CEFORANIDE	1984-05-24	Discontinued	No
			005	PRECEF	INJECTABLE;INJECTION	20GM/VIAL	CEFORANIDE	1984-05-24	Discontinued	No
062336	ANDA	BRISTOL MYERS	001	MUTAMYCIN	INJECTABLE;INJECTION	5MG/VIAL	MITOMYCIN	1981-08-24	Discontinued	No
			002	MUTAMYCIN	INJECTABLE;INJECTION	20MG/VIAL	MITOMYCIN	1981-08-24	Discontinued	No
			003	MUTAMYCIN	INJECTABLE;INJECTION	40MG/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MITOMYCIN	1981-08-24	Discontinued	No
086358	ANDA	BRISTOL	001	MEXATE	INJECTABLE;INJECTION	EQ 20MG BASE/VIAL	METHOTREXATE SODIUM	1979-09-05	Discontinued	No
			002	MEXATE	INJECTABLE;INJECTION	EQ 50MG BASE/VIAL	METHOTREXATE SODIUM	1979-09-05	Discontinued	No
			003	MEXATE	INJECTABLE;INJECTION	EQ 100MG BASE/VIAL	METHOTREXATE SODIUM	1979-09-05	Discontinued	No
			004	MEXATE	INJECTABLE;INJECTION	EQ 250MG BASE/VIAL	METHOTREXATE SODIUM	1979-09-05	Discontinued	No
086454	ANDA	BRISTOL MYERS SQUIBB	001	AMITID	TABLET;ORAL	10MG	AMITRIPTYLINE HYDROCHLORIDE	1978-10-19	Discontinued	No
			002	AMITID	TABLET;ORAL	25MG	AMITRIPTYLINE HYDROCHLORIDE	1978-10-19	Discontinued	No
			003	AMITID	TABLET;ORAL	50MG	AMITRIPTYLINE HYDROCHLORIDE	1978-10-19	Discontinued	No
			004	AMITID	TABLET;ORAL	75MG	AMITRIPTYLINE HYDROCHLORIDE	1978-10-19	Discontinued	No
			005	AMITID	TABLET;ORAL	100MG	AMITRIPTYLINE HYDROCHLORIDE	1978-10-19	Discontinued	No
017907	NDA	BRISTOL MYERS SQUIBB	001	GLUCOSCAN	INJECTABLE;INJECTION	N/A	TECHNETIUM TC-99M GLUCEPTATE KIT	1978-05-25	Discontinued	No
085910	ANDA	BRISTOL MYERS SQUIBB	001	OXYCODONE 2.5/APAP 500	TABLET;ORAL	500MG;2.5MG	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	1977-10-25	Discontinued	No
085911	ANDA	BRISTOL MYERS SQUIBB	001	OXYCODONE 5/APAP 500	TABLET;ORAL	500MG;5MG	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	1977-10-25	Discontinued	No
084499	ANDA	BRISTOL MYERS SQUIBB	001	ESTRACE	TABLET;ORAL	1MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ESTRADIOL	1975-07-28	Discontinued	No
084500	ANDA	BRISTOL MYERS SQUIBB	001	ESTRACE	TABLET;ORAL	2MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ESTRADIOL	1975-07-23	Discontinued	No
061888	ANDA	BRISTOL	001	BRISTACYCLINE	CAPSULE;ORAL	250MG	TETRACYCLINE HYDROCHLORIDE	1974-12-05	Discontinued	No
061888	ANDA	BRISTOL	002	BRISTACYCLINE	CAPSULE;ORAL	500MG	TETRACYCLINE HYDROCHLORIDE	1974-12-05	Discontinued	No
061887	ANDA	BRISTOL	001	BRISTAMYCIN	TABLET;ORAL	EQ 250MG BASE	ERYTHROMYCIN STEARATE	1974-12-05	Discontinued	No
061889	ANDA	BRISTOL	001	TETREX	CAPSULE;ORAL	EQ 500MG HYDROCHLORIDE	TETRACYCLINE PHOSPHATE COMPLEX	1974-12-05	Discontinued	No
061889	ANDA	BRISTOL	002	TETREX	CAPSULE;ORAL	EQ 250MG HYDROCHLORIDE	TETRACYCLINE PHOSPHATE COMPLEX	1974-12-05	Discontinued	No
016640	NDA	BRISTOL MYERS	001	QUESTRAN	POWDER;ORAL	EQ 4GM RESIN/PACKET Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CHOLESTYRAMINE	1973-08-03	Discontinued	No
016640	NDA	BRISTOL MYERS	003	QUESTRAN	POWDER;ORAL	EQ 4GM RESIN/SCOOPFUL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CHOLESTYRAMINE	1973-08-03	Discontinued	No
050443	NDA	BRISTOL MYERS SQUIBB	001	BLENOXANE	INJECTABLE;INJECTION	EQ 15 UNITS BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	BLEOMYCIN SULFATE	1973-07-31	Discontinued	No
050443	NDA	BRISTOL MYERS SQUIBB	002	BLENOXANE	INJECTABLE;INJECTION	EQ 30 UNITS BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	BLEOMYCIN SULFATE	1973-07-31	Discontinued	No
061658	ANDA	BRISTOL	001	BRISTACYCLINE	CAPSULE;ORAL	250MG	TETRACYCLINE HYDROCHLORIDE	1972-06-28	Discontinued	No
061658	ANDA	BRISTOL	002	BRISTACYCLINE	CAPSULE;ORAL	500MG	TETRACYCLINE HYDROCHLORIDE	1972-06-28	Discontinued	No
061653	ANDA	BRISTOL	001	TETREX	CAPSULE;ORAL	EQ 100MG HYDROCHLORIDE	TETRACYCLINE PHOSPHATE COMPLEX	1972-06-20	Discontinued	No
			002	TETREX	CAPSULE;ORAL	EQ 250MG HYDROCHLORIDE	TETRACYCLINE PHOSPHATE COMPLEX	1972-06-20	Discontinued	No
			003	TETREX	CAPSULE;ORAL	EQ 500MG HYDROCHLORIDE	TETRACYCLINE PHOSPHATE COMPLEX	1972-06-20	Discontinued	No
016727	NDA	BRISTOL MYERS SQUIBB	001	PROLIXIN DECANOATE	INJECTABLE;INJECTION	25MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	FLUPHENAZINE DECANOATE	1972-06-20	Discontinued	No
016979	NDA	BRISTOL MYERS SQUIBB	001	MEGACE	TABLET;ORAL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MEGESTROL ACETATE	1971-08-18	Discontinued	No
016979	NDA	BRISTOL MYERS SQUIBB	002	MEGACE	TABLET;ORAL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MEGESTROL ACETATE	1971-08-18	Discontinued	No
050341	NDA	BRISTOL MYERS SQUIBB	003	FUNGIZONE	SUSPENSION;ORAL	100MG/ML	AMPHOTERICIN B	1971-06-02	Discontinued	No
061396	ANDA	BRISTOL	001	VERSAPEN-K	CAPSULE;ORAL	EQ 225MG AMPICIL	HETACILLIN POTASSIUM	1971-03-03	Discontinued	No
061396	ANDA	BRISTOL	002	VERSAPEN-K	CAPSULE;ORAL	EQ 450MG AMPICIL	HETACILLIN POTASSIUM	1971-03-03	Discontinued	No
061392	ANDA	BRISTOL MYERS SQUIBB	001	PRINCIPEN	CAPSULE;ORAL	EQ 250MG BASE	AMPICILLIN/AMPICILLIN TRIHYDRATE	1971-03-03	Discontinued	No
061392	ANDA	BRISTOL MYERS SQUIBB	002	PRINCIPEN	CAPSULE;ORAL	EQ 500MG BASE	AMPICILLIN/AMPICILLIN TRIHYDRATE	1971-03-03	Discontinued	No
016118	NDA	BRISTOL MYERS SQUIBB	001	TESLAC	TABLET;ORAL	50MG	TESTOLACTONE	1970-05-27	Discontinued	No
016118	NDA	BRISTOL MYERS SQUIBB	002	TESLAC	TABLET;ORAL	250MG	TESTOLACTONE	1970-05-27	Discontinued	No
061150	ANDA	BRISTOL	001	BETAPEN-VK	TABLET;ORAL	EQ 250MG BASE	PENICILLIN V POTASSIUM		Discontinued	No
061150	ANDA	BRISTOL	002	BETAPEN-VK	TABLET;ORAL	EQ 500MG BASE	PENICILLIN V POTASSIUM		Discontinued	No
062288	ANDA	BRISTOL	001	BRISTAGEN	INJECTABLE;INJECTION	EQ 40MG BASE/ML	GENTAMICIN SULFATE		Discontinued	No
061304	ANDA	BRISTOL	001	BRISTAMYCIN	TABLET;ORAL	EQ 250MG BASE	ERYTHROMYCIN STEARATE		Discontinued	No
062464	ANDA	BRISTOL	001	CEPHALOTHIN SODIUM	INJECTABLE;INJECTION	EQ 1GM BASE/VIAL	CEPHALOTHIN SODIUM		Discontinued	No
			002	CEPHALOTHIN SODIUM	INJECTABLE;INJECTION	EQ 2GM BASE/VIAL	CEPHALOTHIN SODIUM		Discontinued	No
			003	CEPHALOTHIN SODIUM	INJECTABLE;INJECTION	EQ 4GM BASE/VIAL	CEPHALOTHIN SODIUM		Discontinued	No
050450	NDA	BRISTOL	001	MUTAMYCIN	INJECTABLE;INJECTION	5MG/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MITOMYCIN		Discontinued	No
050450	NDA	BRISTOL	002	MUTAMYCIN	INJECTABLE;INJECTION	20MG/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MITOMYCIN		Discontinued	No
050093	NDA	BRISTOL	001	POLYCILLIN	TABLET, CHEWABLE;ORAL	EQ 125MG BASE	AMPICILLIN/AMPICILLIN TRIHYDRATE		Discontinued	No
050308	NDA	BRISTOL	001	POLYCILLIN	FOR SUSPENSION;ORAL	EQ 125MG BASE/5ML	AMPICILLIN/AMPICILLIN TRIHYDRATE		Discontinued	No
			002	POLYCILLIN	FOR SUSPENSION;ORAL	EQ 250MG BASE/5ML	AMPICILLIN/AMPICILLIN TRIHYDRATE		Discontinued	No
			003	POLYCILLIN	FOR SUSPENSION;ORAL	EQ 500MG BASE/5ML	AMPICILLIN/AMPICILLIN TRIHYDRATE		Discontinued	No
			004	POLYCILLIN	FOR SUSPENSION;ORAL	EQ 100MG BASE/ML	AMPICILLIN/AMPICILLIN TRIHYDRATE		Discontinued	No
050310	NDA	BRISTOL	001	POLYCILLIN	CAPSULE;ORAL	EQ 250MG BASE	AMPICILLIN/AMPICILLIN TRIHYDRATE		Discontinued	No
050310	NDA	BRISTOL	002	POLYCILLIN	CAPSULE;ORAL	EQ 500MG BASE	AMPICILLIN/AMPICILLIN TRIHYDRATE		Discontinued	No
050309	NDA	BRISTOL	001	POLYCILLIN-N	INJECTABLE;INJECTION	EQ 125MG BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	AMPICILLIN SODIUM		Discontinued	No
			002	POLYCILLIN-N	INJECTABLE;INJECTION	EQ 250MG BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	AMPICILLIN SODIUM		Discontinued	No
			003	POLYCILLIN-N	INJECTABLE;INJECTION	EQ 500MG BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	AMPICILLIN SODIUM		Discontinued	No
			004	POLYCILLIN-N	INJECTABLE;INJECTION	EQ 1GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	AMPICILLIN SODIUM		Discontinued	No
			005	POLYCILLIN-N	INJECTABLE;INJECTION	EQ 2GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	AMPICILLIN SODIUM		Discontinued	No
050457	NDA	BRISTOL	001	POLYCILLIN-PRB	FOR SUSPENSION;ORAL	EQ 3.5GM BASE/BOT;1GM/BOT	AMPICILLIN/AMPICILLIN TRIHYDRATE; PROBENECID		Discontinued	No
062376	ANDA	BRISTOL	001	ULTRACEF	FOR SUSPENSION;ORAL	EQ 125MG BASE/5ML	CEFADROXIL/CEFADROXIL HEMIHYDRATE		Discontinued	No
			002	ULTRACEF	FOR SUSPENSION;ORAL	EQ 250MG BASE/5ML	CEFADROXIL/CEFADROXIL HEMIHYDRATE		Discontinued	No
			003	ULTRACEF	FOR SUSPENSION;ORAL	EQ 500MG BASE/5ML	CEFADROXIL/CEFADROXIL HEMIHYDRATE		Discontinued	No
062378	ANDA	BRISTOL	001	ULTRACEF	CAPSULE;ORAL	EQ 500MG BASE	CEFADROXIL/CEFADROXIL HEMIHYDRATE		Discontinued	No
062408	ANDA	BRISTOL	001	ULTRACEF	TABLET;ORAL	EQ 1GM BASE	CEFADROXIL/CEFADROXIL HEMIHYDRATE		Discontinued	No
050060	NDA	BRISTOL	001	VERSAPEN	FOR SUSPENSION;ORAL	EQ 112.5MG AMPICIL/5ML	HETACILLIN		Discontinued	No
050060	NDA	BRISTOL	003	VERSAPEN	FOR SUSPENSION;ORAL	EQ 112.5MG AMPICIL/ML	HETACILLIN		Discontinued	No
061398	ANDA	BRISTOL	001	VERSAPEN	FOR SUSPENSION;ORAL	EQ 112.5MG AMPICIL/ML	HETACILLIN		Discontinued	No
061398	ANDA	BRISTOL	002	VERSAPEN	FOR SUSPENSION;ORAL	EQ 225MG AMPICIL/5ML	HETACILLIN		Discontinued	No
083266	ANDA	BRISTOL MYERS SQUIBB	001	AMNESTROGEN	TABLET;ORAL	0.3MG	ESTROGENS, ESTERIFIED		Discontinued	No
			002	AMNESTROGEN	TABLET;ORAL	0.625MG	ESTROGENS, ESTERIFIED		Discontinued	No
			003	AMNESTROGEN	TABLET;ORAL	1.25MG	ESTROGENS, ESTERIFIED		Discontinued	No
			004	AMNESTROGEN	TABLET;ORAL	2.5MG	ESTROGENS, ESTERIFIED		Discontinued	No
062908	ANDA	BRISTOL MYERS SQUIBB	001	CLINDAMYCIN PHOSPHATE	INJECTABLE;INJECTION	EQ 150MG BASE/ML	CLINDAMYCIN PHOSPHATE		Discontinued	No
085020	ANDA	BRISTOL MYERS SQUIBB	002	DEAPRIL-ST	TABLET;SUBLINGUAL	1MG	ERGOLOID MESYLATES		Discontinued	No
010347	NDA	BRISTOL MYERS SQUIBB	002	DELALUTIN	SOLUTION;INTRAMUSCULAR	250MG/ML (250MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	HYDROXYPROGESTERONE CAPROATE		Discontinued	No
010347	NDA	BRISTOL MYERS SQUIBB	004	DELALUTIN	SOLUTION;INTRAMUSCULAR	125MG/ML (125MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	HYDROXYPROGESTERONE CAPROATE		Discontinued	No
016911	NDA	BRISTOL MYERS SQUIBB	001	DELALUTIN	SOLUTION;INTRAMUSCULAR	125MG/ML (125MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	HYDROXYPROGESTERONE CAPROATE		Discontinued	No
016911	NDA	BRISTOL MYERS SQUIBB	002	DELALUTIN	SOLUTION;INTRAMUSCULAR	250MG/ML (250MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	HYDROXYPROGESTERONE CAPROATE		Discontinued	No
061605	ANDA	BRISTOL MYERS SQUIBB	001	ETHRIL 250	TABLET;ORAL	EQ 250MG BASE	ERYTHROMYCIN STEARATE		Discontinued	No
061605	ANDA	BRISTOL MYERS SQUIBB	002	ETHRIL 500	TABLET;ORAL	EQ 500MG BASE	ERYTHROMYCIN STEARATE		Discontinued	No
018125	NDA	BRISTOL MYERS SQUIBB	001	HALOG	OINTMENT;TOPICAL	0.025%	HALCINONIDE		Discontinued	No
060365	ANDA	BRISTOL MYERS SQUIBB	001	NEOMYCIN SULFATE	TABLET;ORAL	500MG	NEOMYCIN SULFATE		Discontinued	No
008392	NDA	BRISTOL MYERS SQUIBB	003	NYDRAZID	TABLET;ORAL	100MG	ISONIAZID		Discontinued	No
011359	NDA	BRISTOL MYERS SQUIBB	001	ORA-TESTRYL	TABLET;ORAL	2MG	FLUOXYMESTERONE		Discontinued	No
011359	NDA	BRISTOL MYERS SQUIBB	002	ORA-TESTRYL	TABLET;ORAL	5MG	FLUOXYMESTERONE		Discontinued	No
061935	ANDA	BRISTOL MYERS SQUIBB	001	PENICILLIN G SODIUM	INJECTABLE;INJECTION	5,000,000 UNITS/VIAL	PENICILLIN G SODIUM		Discontinued	No
009357	NDA	BRISTOL MYERS SQUIBB	001	RAU-SED	TABLET;ORAL	0.1MG	RESERPINE		Discontinued	No
			004	RAU-SED	TABLET;ORAL	0.25MG	RESERPINE		Discontinued	No
			006	RAU-SED	TABLET;ORAL	0.5MG	RESERPINE		Discontinued	No
			008	RAU-SED	TABLET;ORAL	1MG	RESERPINE		Discontinued	No
083176	ANDA	BRISTOL MYERS SQUIBB	001	REMSED	TABLET;ORAL	50MG	PROMETHAZINE HYDROCHLORIDE		Discontinued	No
083176	ANDA	BRISTOL MYERS SQUIBB	002	REMSED	TABLET;ORAL	25MG	PROMETHAZINE HYDROCHLORIDE		Discontinued	No
009052	NDA	BRISTOL MYERS SQUIBB	001	REZIPAS	POWDER;ORAL	EQ 500MG BASE/GM	AMINOSALICYLIC ACID RESIN COMPLEX		Discontinued	No
004056	NDA	BRISTOL MYERS SQUIBB	001	STILBESTROL	SUPPOSITORY;VAGINAL	0.1MG	DIETHYLSTILBESTROL		Discontinued	No
			002	STILBESTROL	SUPPOSITORY;VAGINAL	0.5MG	DIETHYLSTILBESTROL		Discontinued	No
			003	STILBESTROL	INJECTABLE;INJECTION	0.2MG/ML	DIETHYLSTILBESTROL		Discontinued	No
			004	STILBESTROL	INJECTABLE;INJECTION	0.5MG/ML	DIETHYLSTILBESTROL		Discontinued	No
			005	STILBESTROL	INJECTABLE;INJECTION	1MG/ML	DIETHYLSTILBESTROL		Discontinued	No
			006	STILBESTROL	INJECTABLE;INJECTION	5MG/ML	DIETHYLSTILBESTROL		Discontinued	No
			007	STILBETIN	TABLET;ORAL	0.1MG	DIETHYLSTILBESTROL		Discontinued	No
			008	STILBETIN	TABLET;ORAL	0.5MG	DIETHYLSTILBESTROL		Discontinued	No
			009	STILBETIN	TABLET;ORAL	1MG	DIETHYLSTILBESTROL		Discontinued	No
			010	STILBETIN	TABLET;ORAL	5MG	DIETHYLSTILBESTROL		Discontinued	No
			011	STILBETIN	TABLET, DELAYED RELEASE;ORAL	0.1MG	DIETHYLSTILBESTROL		Discontinued	No
			012	STILBETIN	TABLET, DELAYED RELEASE;ORAL	0.5MG	DIETHYLSTILBESTROL		Discontinued	No
			013	STILBETIN	TABLET, DELAYED RELEASE;ORAL	1MG	DIETHYLSTILBESTROL		Discontinued	No
			014	STILBETIN	TABLET, DELAYED RELEASE;ORAL	5MG	DIETHYLSTILBESTROL		Discontinued	No
			017	STILBETIN	TABLET;ORAL	0.25MG	DIETHYLSTILBESTROL		Discontinued	No
006904	NDA	BRISTOL MYERS SQUIBB	001	TERFONYL	TABLET;ORAL	167MG;167MG;167MG	TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE)		Discontinued	No
006904	NDA	BRISTOL MYERS SQUIBB	002	TERFONYL	SUSPENSION;ORAL	167MG/5ML;167MG/5ML;167MG/5ML	TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE)		Discontinued	No
050530	NDA	BRISTOL MYERS SQUIBB	001	VELOSEF	TABLET;ORAL	1GM	CEPHRADINE		Discontinued	No
080860	ANDA	BRISTOL MYERS SQUIBB	001	VITAMIN A	CAPSULE;ORAL	EQ 50,000 UNITS BASE	VITAMIN A PALMITATE		Discontinued	No
016119	NDA	BRISTOL MYERS SQUIBB	001	TESLAC	INJECTABLE;INJECTION	100MG/ML	TESTOLACTONE	1969-06-03	Discontinued	No
011123	NDA	BRISTOL MYERS SQUIBB	001	VESPRIN	TABLET;ORAL	10MG	TRIFLUPROMAZINE HYDROCHLORIDE	1957-09-16	Discontinued	No
			002	VESPRIN	TABLET;ORAL	25MG	TRIFLUPROMAZINE HYDROCHLORIDE	1957-09-16	Discontinued	No
			003	VESPRIN	TABLET;ORAL	50MG	TRIFLUPROMAZINE HYDROCHLORIDE	1957-09-16	Discontinued	No
050212	NDA	BRISTOL	002	TETREX	CAPSULE;ORAL	EQ 250MG HYDROCHLORIDE	TETRACYCLINE PHOSPHATE COMPLEX	1957-02-19	Discontinued	No
050212	NDA	BRISTOL	003	TETREX	CAPSULE;ORAL	EQ 500MG HYDROCHLORIDE	TETRACYCLINE PHOSPHATE COMPLEX	1957-02-19	Discontinued	No
009218	NDA	BRISTOL MYERS SQUIBB	005	COUMADIN	TABLET;ORAL	10MG	WARFARIN SODIUM	1954-06-08	Discontinued	No
			007	COUMADIN	TABLET;ORAL	5MG	WARFARIN SODIUM	1954-06-08	Discontinued	No
			012	COUMADIN	INJECTABLE;INJECTION	75MG/VIAL	WARFARIN SODIUM	1954-06-08	Discontinued	No
			013	COUMADIN	TABLET;ORAL	2MG	WARFARIN SODIUM	1954-06-08	Discontinued	No
			016	COUMADIN	TABLET;ORAL	7.5MG	WARFARIN SODIUM	1954-06-08	Discontinued	No
			018	COUMADIN	TABLET;ORAL	2.5MG	WARFARIN SODIUM	1954-06-08	Discontinued	No
			020	COUMADIN	INJECTABLE;INJECTION	50MG/VIAL	WARFARIN SODIUM	1954-06-08	Discontinued	No
			022	COUMADIN	TABLET;ORAL	1MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	WARFARIN SODIUM	1954-06-08	Discontinued	No
			023	COUMADIN	TABLET;ORAL	4MG	WARFARIN SODIUM	1954-06-08	Discontinued	No
			024	COUMADIN	INJECTABLE;INJECTION	5MG/VIAL	WARFARIN SODIUM	1954-06-08	Discontinued	No
			025	COUMADIN	TABLET;ORAL	3MG	WARFARIN SODIUM	1954-06-08	Discontinued	No
			026	COUMADIN	TABLET;ORAL	6MG	WARFARIN SODIUM	1954-06-08	Discontinued	No
006799	NDA	BRISTOL MYERS SQUIBB	002	RUBRAMIN PC	INJECTABLE;INJECTION	0.1MG/ML	CYANOCOBALAMIN	1950-09-29	Discontinued	No
			004	RUBRAMIN PC	INJECTABLE;INJECTION	1MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CYANOCOBALAMIN	1950-09-29	Discontinued	No
			010	RUBRAMIN PC	INJECTABLE;INJECTION	1MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CYANOCOBALAMIN	1950-09-29	Discontinued	No
005657	NDA	BRISTOL MYERS SQUIBB	001	TUBOCURARINE CHLORIDE	INJECTABLE;INJECTION	3MG/ML	TUBOCURARINE CHLORIDE	1945-02-20	Discontinued	No