FDA Approved Products

Application #	Type	Sponsor	Product #	Drug Name	Form	Strength	Active Ingredient	Approval Date	Marketing Status	Reference Standard
216632	NDA	BAUSCH	001	CABTREO	GEL;TOPICAL	0.15%;3.1%;1.2%	ADAPALENE; BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE	2023-10-20	Prescription	Yes
211882	NDA	BAUSCH	001	ARAZLO	LOTION;TOPICAL	0.045%	TAZAROTENE	2019-12-18	Prescription	Yes
209354	NDA	BAUSCH	001	DUOBRII	LOTION;TOPICAL	0.01%;0.045%	HALOBETASOL PROPIONATE; TAZAROTENE	2019-04-25	Prescription	Yes
209355	NDA	BAUSCH	001	BRYHALI	LOTION;TOPICAL	0.01%	HALOBETASOL PROPIONATE	2018-11-06	Prescription	Yes
203567	NDA	BAUSCH	001	JUBLIA	SOLUTION;TOPICAL	10%	EFINACONAZOLE	2014-06-06	Prescription	Yes
204153	NDA	BAUSCH	001	LUZU	CREAM;TOPICAL	1%	LULICONAZOLE	2013-11-14	Prescription	Yes
090715	ANDA	BAUSCH	001	FENOFIBRATE	TABLET;ORAL	48MG	FENOFIBRATE	2012-04-05	Discontinued	No
090715	ANDA	BAUSCH	002	FENOFIBRATE	TABLET;ORAL	145MG	FENOFIBRATE	2012-04-05	Discontinued	No
022483	NDA	BAUSCH	001	ZYCLARA	CREAM;TOPICAL	3.75%	IMIQUIMOD	2010-03-25	Prescription	Yes
022483	NDA	BAUSCH	002	ZYCLARA	CREAM;TOPICAL	2.5%	IMIQUIMOD	2010-03-25	Prescription	Yes
022436	NDA	BAUSCH	001	XERESE	CREAM;TOPICAL	5%;1%	ACYCLOVIR; HYDROCORTISONE	2009-07-31	Prescription	Yes
050819	NDA	BAUSCH	001	ACANYA	GEL;TOPICAL	2.5%;EQ 1.2% BASE	BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE	2008-10-23	Prescription	Yes
050819	NDA	BAUSCH	002	ONEXTON	GEL;TOPICAL	3.75%;EQ 1.2% BASE	BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE	2008-10-23	Prescription	Yes
040700	ANDA	BAUSCH	001	DEXAMETHASONE	TABLET;ORAL	1.5MG	DEXAMETHASONE	2008-08-15	Discontinued	No
021894	NDA	BAUSCH	001	XENAZINE	TABLET;ORAL	12.5MG	TETRABENAZINE	2008-08-15	Prescription	No
021894	NDA	BAUSCH	002	XENAZINE	TABLET;ORAL	25MG	TETRABENAZINE	2008-08-15	Prescription	Yes
022108	NDA	BAUSCH	001	APLENZIN	TABLET, EXTENDED RELEASE;ORAL	174MG	BUPROPION HYDROBROMIDE	2008-04-23	Prescription	No
			002	APLENZIN	TABLET, EXTENDED RELEASE;ORAL	348MG	BUPROPION HYDROBROMIDE	2008-04-23	Prescription	No
			003	APLENZIN	TABLET, EXTENDED RELEASE;ORAL	522MG	BUPROPION HYDROBROMIDE	2008-04-23	Prescription	Yes
022076	NDA	BAUSCH	001	LOCOID	LOTION;TOPICAL	0.1%	HYDROCORTISONE BUTYRATE	2007-05-18	Discontinued	No
050802	NDA	BAUSCH	001	ZIANA	GEL;TOPICAL	1.2%;0.025%	CLINDAMYCIN PHOSPHATE; TRETINOIN	2006-11-07	Prescription	Yes
021479	NDA	BAUSCH	001	ZELAPAR	TABLET, ORALLY DISINTEGRATING;ORAL	1.25MG	SELEGILINE HYDROCHLORIDE	2006-06-14	Prescription	Yes
050808	NDA	BAUSCH	001	SOLODYN	TABLET, EXTENDED RELEASE;ORAL	EQ 45MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MINOCYCLINE HYDROCHLORIDE	2006-05-08	Discontinued	No
			002	SOLODYN	TABLET, EXTENDED RELEASE;ORAL	EQ 90MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MINOCYCLINE HYDROCHLORIDE	2006-05-08	Discontinued	No
			003	SOLODYN	TABLET, EXTENDED RELEASE;ORAL	EQ 135MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MINOCYCLINE HYDROCHLORIDE	2006-05-08	Discontinued	No
			004	SOLODYN	TABLET, EXTENDED RELEASE;ORAL	EQ 65MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MINOCYCLINE HYDROCHLORIDE	2006-05-08	Discontinued	No
			005	SOLODYN	TABLET, EXTENDED RELEASE;ORAL	EQ 115MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MINOCYCLINE HYDROCHLORIDE	2006-05-08	Discontinued	No
			006	SOLODYN	TABLET, EXTENDED RELEASE;ORAL	EQ 105MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MINOCYCLINE HYDROCHLORIDE	2006-05-08	Discontinued	No
			007	SOLODYN	TABLET, EXTENDED RELEASE;ORAL	EQ 80MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MINOCYCLINE HYDROCHLORIDE	2006-05-08	Discontinued	No
			008	SOLODYN	TABLET, EXTENDED RELEASE;ORAL	EQ 55MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MINOCYCLINE HYDROCHLORIDE	2006-05-08	Discontinued	No
065281	ANDA	BAUSCH	001	DOXYCYCLINE HYCLATE	CAPSULE, DELAYED RELEASE;ORAL	EQ 75MG BASE	DOXYCYCLINE HYCLATE	2005-12-21	Discontinued	No
065281	ANDA	BAUSCH	002	DOXYCYCLINE HYCLATE	CAPSULE, DELAYED RELEASE;ORAL	EQ 100MG BASE	DOXYCYCLINE HYCLATE	2005-12-21	Discontinued	No
020645	NDA	BAUSCH	001	AMMONUL	SOLUTION;INTRAVENOUS	10%;10% (5GM/50ML;5GM/50ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	SODIUM BENZOATE; SODIUM PHENYLACETATE	2005-02-17	Discontinued	No
021758	NDA	BAUSCH	001	VANOS	CREAM;TOPICAL	0.1%	FLUOCINONIDE	2005-02-11	Prescription	Yes
021515	NDA	BAUSCH	001	WELLBUTRIN XL	TABLET, EXTENDED RELEASE;ORAL	150MG	BUPROPION HYDROCHLORIDE	2003-08-28	Prescription	No
021515	NDA	BAUSCH	002	WELLBUTRIN XL	TABLET, EXTENDED RELEASE;ORAL	300MG	BUPROPION HYDROCHLORIDE	2003-08-28	Prescription	Yes
021271	BLA	BAUSCH	001	IPRIVASK	INJECTABLE;SUBCUTANEOUS	15MG/VIAL	DESIRUDIN RECOMBINANT	2003-04-04	Discontinued	No
076025	ANDA	BAUSCH	001	IPRATROPIUM BROMIDE	SPRAY, METERED;NASAL	0.021MG/SPRAY	IPRATROPIUM BROMIDE	2003-03-31	Prescription	No
076103	ANDA	BAUSCH	001	IPRATROPIUM BROMIDE	SPRAY, METERED;NASAL	0.042MG/SPRAY	IPRATROPIUM BROMIDE	2003-03-31	Prescription	No
021159	NDA	BAUSCH	001	LOPROX	SHAMPOO;TOPICAL	1%	CICLOPIROX	2003-02-28	Discontinued	No
021392	NDA	BAUSCH	001	CARDIZEM LA	TABLET, EXTENDED RELEASE;ORAL	120MG	DILTIAZEM HYDROCHLORIDE	2003-02-06	Prescription	No
			002	CARDIZEM LA	TABLET, EXTENDED RELEASE;ORAL	180MG	DILTIAZEM HYDROCHLORIDE	2003-02-06	Prescription	No
			003	CARDIZEM LA	TABLET, EXTENDED RELEASE;ORAL	240MG	DILTIAZEM HYDROCHLORIDE	2003-02-06	Prescription	No
			004	CARDIZEM LA	TABLET, EXTENDED RELEASE;ORAL	300MG	DILTIAZEM HYDROCHLORIDE	2003-02-06	Prescription	No
			005	CARDIZEM LA	TABLET, EXTENDED RELEASE;ORAL	360MG	DILTIAZEM HYDROCHLORIDE	2003-02-06	Prescription	No
			006	CARDIZEM LA	TABLET, EXTENDED RELEASE;ORAL	420MG	DILTIAZEM HYDROCHLORIDE	2003-02-06	Prescription	Yes
021478	NDA	BAUSCH	001	ZOVIRAX	CREAM;TOPICAL	5%	ACYCLOVIR	2002-12-30	Prescription	No
075250	ANDA	BAUSCH	001	PREDNISOLONE SODIUM PHOSPHATE	SOLUTION;ORAL	EQ 15MG BASE/5ML	PREDNISOLONE SODIUM PHOSPHATE	2002-07-12	Discontinued	No
074805	ANDA	BAUSCH	001	FLUNISOLIDE	SPRAY, METERED;NASAL	0.025MG/SPRAY	FLUNISOLIDE	2002-02-20	Prescription	Yes
021302	NDA	BAUSCH	001	ELIDEL	CREAM;TOPICAL	1%	PIMECROLIMUS	2001-12-13	Prescription	Yes
075835	ANDA	BAUSCH	001	IPRATROPIUM BROMIDE	SOLUTION;INHALATION	0.02%	IPRATROPIUM BROMIDE	2001-10-15	Discontinued	No
050756	NDA	BAUSCH	001	BENZACLIN	GEL;TOPICAL	5%;EQ 1% BASE	BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE	2000-12-21	Discontinued	No
050756	NDA	BAUSCH	002	BENZACLIN	GEL;TOPICAL	5%;EQ 1% BASE	BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE	2000-12-21	Discontinued	No
075585	ANDA	BAUSCH	001	CROMOLYN SODIUM	SOLUTION;INHALATION	10MG/ML	CROMOLYN SODIUM	2000-12-21	Discontinued	No
050782	NDA	BAUSCH	001	CLINDAGEL	GEL;TOPICAL	EQ 1% BASE	CLINDAMYCIN PHOSPHATE	2000-11-27	Prescription	Yes
021056	NDA	BAUSCH	001	TARGRETIN	GEL;TOPICAL	1%	BEXAROTENE	2000-06-28	Prescription	Yes
075358	ANDA	BAUSCH	001	ALBUTEROL SULFATE	SOLUTION;INHALATION	EQ 0.083% BASE	ALBUTEROL SULFATE	2000-03-29	Discontinued	No
074830	ANDA	BAUSCH	001	DESMOPRESSIN ACETATE	SPRAY, METERED;NASAL	0.01MG/SPRAY	DESMOPRESSIN ACETATE	1999-01-25	Prescription	Yes
075028	ANDA	BAUSCH	001	PENTOXIFYLLINE	TABLET, EXTENDED RELEASE;ORAL	400MG	PENTOXIFYLLINE	1998-07-20	Discontinued	No
075050	ANDA	BAUSCH	001	ALBUTEROL SULFATE	SOLUTION;INHALATION	EQ 0.5% BASE	ALBUTEROL SULFATE	1998-06-18	Discontinued	No
020697	NDA	BAUSCH	001	TASMAR	TABLET;ORAL	100MG	TOLCAPONE	1998-01-29	Prescription	Yes
020697	NDA	BAUSCH	002	TASMAR	TABLET;ORAL	200MG	TOLCAPONE	1998-01-29	Discontinued	No
020148	NDA	BAUSCH	001	MIGRANAL	SPRAY, METERED;NASAL	0.5MG/SPRAY	DIHYDROERGOTAMINE MESYLATE	1997-12-08	Prescription	Yes
020743	NDA	BAUSCH	001	NORITATE	CREAM;TOPICAL	1%	METRONIDAZOLE	1997-09-26	Prescription	Yes
020648	NDA	BAUSCH	001	DIASTAT	GEL;RECTAL	2.5MG/0.5ML (5MG/ML)	DIAZEPAM	1997-07-29	Prescription	Yes
			002	DIASTAT	GEL;RECTAL	5MG/ML (5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DIAZEPAM	1997-07-29	Discontinued	No
			003	DIASTAT	GEL;RECTAL	10MG/2ML (5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DIAZEPAM	1997-07-29	Discontinued	No
			004	DIASTAT	GEL;RECTAL	15MG/3ML (5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DIAZEPAM	1997-07-29	Discontinued	No
			005	DIASTAT	GEL;RECTAL	20MG/4ML (5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DIAZEPAM	1997-07-29	Discontinued	No
			006	DIASTAT ACUDIAL	GEL;RECTAL	20MG/4ML (5MG/ML)	DIAZEPAM	1997-07-29	Prescription	Yes
			007	DIASTAT ACUDIAL	GEL;RECTAL	10MG/2ML (5MG/ML)	DIAZEPAM	1997-07-29	Prescription	Yes
020723	NDA	BAUSCH	001	ALDARA	CREAM;TOPICAL	5% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	IMIQUIMOD	1997-02-27	Discontinued	No
020475	NDA	BAUSCH	001	RETIN-A MICRO	GEL;TOPICAL	0.1%	TRETINOIN	1997-02-07	Prescription	Yes
			002	RETIN-A MICRO	GEL;TOPICAL	0.04%	TRETINOIN	1997-02-07	Prescription	Yes
			003	RETIN-A-MICRO	GEL;TOPICAL	0.08%	TRETINOIN	1997-02-07	Prescription	Yes
			004	RETIN-A-MICRO	GEL;TOPICAL	0.06%	TRETINOIN	1997-02-07	Prescription	Yes
019931	NDA	BAUSCH	001	KLARON	LOTION;TOPICAL	10%	SULFACETAMIDE SODIUM	1996-12-23	Prescription	Yes
089773	ANDA	BAUSCH	001	MINITRAN	FILM, EXTENDED RELEASE;TRANSDERMAL	0.4MG/HR	NITROGLYCERIN	1996-08-30	Discontinued	No
020401	NDA	BAUSCH	001	TIAZAC	CAPSULE, EXTENDED RELEASE;ORAL	120MG	DILTIAZEM HYDROCHLORIDE	1995-09-11	Prescription	No
			002	TIAZAC	CAPSULE, EXTENDED RELEASE;ORAL	180MG	DILTIAZEM HYDROCHLORIDE	1995-09-11	Prescription	No
			003	TIAZAC	CAPSULE, EXTENDED RELEASE;ORAL	240MG	DILTIAZEM HYDROCHLORIDE	1995-09-11	Prescription	No
			004	TIAZAC	CAPSULE, EXTENDED RELEASE;ORAL	300MG	DILTIAZEM HYDROCHLORIDE	1995-09-11	Prescription	No
			005	TIAZAC	CAPSULE, EXTENDED RELEASE;ORAL	360MG	DILTIAZEM HYDROCHLORIDE	1995-09-11	Prescription	No
			006	TIAZAC	CAPSULE, EXTENDED RELEASE;ORAL	420MG	DILTIAZEM HYDROCHLORIDE	1995-09-11	Prescription	Yes
064039	ANDA	BAUSCH	001	ERYTHROMYCIN	SOLUTION;TOPICAL	2%	ERYTHROMYCIN	1994-01-27	Discontinued	No
020014	NDA	BAUSCH	001	MAXAIR	AEROSOL, METERED;INHALATION	EQ 0.2MG BASE/INH	PIRBUTEROL ACETATE	1992-11-30	Discontinued	No
020208	NDA	BAUSCH	001	METROGEL-VAGINAL	GEL;VAGINAL	0.75%	METRONIDAZOLE	1992-08-17	Discontinued	No
020062	NDA	BAUSCH	001	CARDIZEM CD	CAPSULE, EXTENDED RELEASE;ORAL	120MG	DILTIAZEM HYDROCHLORIDE	1991-12-27	Prescription	No
			002	CARDIZEM CD	CAPSULE, EXTENDED RELEASE;ORAL	180MG	DILTIAZEM HYDROCHLORIDE	1991-12-27	Prescription	No
			003	CARDIZEM CD	CAPSULE, EXTENDED RELEASE;ORAL	240MG	DILTIAZEM HYDROCHLORIDE	1991-12-27	Prescription	No
			004	CARDIZEM CD	CAPSULE, EXTENDED RELEASE;ORAL	300MG	DILTIAZEM HYDROCHLORIDE	1991-12-27	Prescription	No
			005	CARDIZEM CD	CAPSULE, EXTENDED RELEASE;ORAL	360MG	DILTIAZEM HYDROCHLORIDE	1991-12-27	Prescription	Yes
050649	NDA	BAUSCH	001	MINOCIN	CAPSULE;ORAL	EQ 50MG BASE	MINOCYCLINE HYDROCHLORIDE	1990-05-31	Prescription	No
			002	MINOCIN	CAPSULE;ORAL	EQ 100MG BASE	MINOCYCLINE HYDROCHLORIDE	1990-05-31	Prescription	No
			003	MINOCIN	CAPSULE;ORAL	EQ 75MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MINOCYCLINE HYDROCHLORIDE	1990-05-31	Discontinued	No
019049	NDA	BAUSCH	001	RETIN-A	CREAM;TOPICAL	0.025%	TRETINOIN	1988-09-16	Prescription	Yes
019116	NDA	BAUSCH	001	LOCOID	SOLUTION;TOPICAL	0.1%	HYDROCORTISONE BUTYRATE	1987-02-25	Prescription	Yes
019009	NDA	BAUSCH	001	MAXAIR	AEROSOL, METERED;INHALATION	EQ 0.2MG BASE/INH	PIRBUTEROL ACETATE	1986-12-30	Discontinued	No
019221	NDA	BAUSCH	001	VASERETIC	TABLET;ORAL	10MG;25MG	ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE	1986-10-31	Prescription	Yes
019221	NDA	BAUSCH	003	VASERETIC	TABLET;ORAL	5MG;12.5MG	ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE	1986-10-31	Prescription	No
019600	NDA	BAUSCH	001	OXSORALEN-ULTRA	CAPSULE;ORAL	10MG	METHOXSALEN	1986-10-30	Prescription	Yes
019462	NDA	BAUSCH	001	PEPCID	TABLET;ORAL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	FAMOTIDINE	1986-10-15	Discontinued	No
019462	NDA	BAUSCH	002	PEPCID	TABLET;ORAL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	FAMOTIDINE	1986-10-15	Discontinued	No
018859	NDA	BAUSCH	001	VIRAZOLE	FOR SOLUTION;INHALATION	6GM/VIAL	RIBAVIRIN	1985-12-31	Discontinued	No
018677	NDA	BAUSCH	001	CESAMET	CAPSULE;ORAL	1MG	NABILONE	1985-12-26	Discontinued	No
018998	NDA	BAUSCH	001	VASOTEC	TABLET;ORAL	5MG	ENALAPRIL MALEATE	1985-12-24	Prescription	No
			002	VASOTEC	TABLET;ORAL	10MG	ENALAPRIL MALEATE	1985-12-24	Prescription	No
			003	VASOTEC	TABLET;ORAL	20MG	ENALAPRIL MALEATE	1985-12-24	Prescription	Yes
			005	VASOTEC	TABLET;ORAL	2.5MG	ENALAPRIL MALEATE	1985-12-24	Prescription	No
019194	NDA	BAUSCH	001	SYPRINE	CAPSULE;ORAL	250MG	TRIENTINE HYDROCHLORIDE	1985-11-08	Prescription	Yes
050584	NDA	BAUSCH	001	AKNE-MYCIN	OINTMENT;TOPICAL	2%	ERYTHROMYCIN	1985-01-10	Discontinued	No
018602	NDA	BAUSCH	001	CARDIZEM	TABLET;ORAL	30MG	DILTIAZEM HYDROCHLORIDE	1982-11-05	Prescription	No
			002	CARDIZEM	TABLET;ORAL	60MG	DILTIAZEM HYDROCHLORIDE	1982-11-05	Prescription	No
			003	CARDIZEM	TABLET;ORAL	90MG	DILTIAZEM HYDROCHLORIDE	1982-11-05	Prescription	No
			004	CARDIZEM	TABLET;ORAL	120MG	DILTIAZEM HYDROCHLORIDE	1982-11-05	Prescription	Yes
018514	NDA	BAUSCH	001	LOCOID	CREAM;TOPICAL	0.1%	HYDROCORTISONE BUTYRATE	1982-03-31	Prescription	Yes
018604	NDA	BAUSCH	001	ZOVIRAX	OINTMENT;TOPICAL	5%	ACYCLOVIR	1982-03-29	Prescription	Yes
087457	ANDA	BAUSCH	001	SYNACORT	CREAM;TOPICAL	2.5%	HYDROCORTISONE	1981-06-23	Discontinued	No
087458	ANDA	BAUSCH	001	SYNACORT	CREAM;TOPICAL	1%	HYDROCORTISONE	1981-06-23	Discontinued	No
087459	ANDA	BAUSCH	001	SYNACORT	CREAM;TOPICAL	0.5%	HYDROCORTISONE	1981-06-23	Discontinued	No
087147	ANDA	BAUSCH	001	ANDROID 25	TABLET;ORAL	25MG	METHYLTESTOSTERONE	1981-02-09	Discontinued	No
017871	NDA	BAUSCH	001	DEMSER	CAPSULE;ORAL	250MG	METYROSINE	1979-10-03	Prescription	Yes
017955	NDA	BAUSCH	001	RETIN-A	GEL;TOPICAL	0.01%	TRETINOIN	1978-10-17	Prescription	Yes
017794	NDA	BAUSCH	001	ATIVAN	TABLET;ORAL	0.5MG	LORAZEPAM	1977-09-30	Prescription	No
			002	ATIVAN	TABLET;ORAL	1MG	LORAZEPAM	1977-09-30	Prescription	No
			003	ATIVAN	TABLET;ORAL	2MG	LORAZEPAM	1977-09-30	Prescription	Yes
085475	ANDA	BAUSCH	001	LIBRIUM	CAPSULE;ORAL	25MG	CHLORDIAZEPOXIDE HYDROCHLORIDE	1977-09-21	Prescription	No
085272	ANDA	BAUSCH	001	BONTRIL PDM	TABLET;ORAL	35MG	PHENDIMETRAZINE TARTRATE	1976-12-22	Prescription	Yes
050475	NDA	BAUSCH	001	GRIS-PEG	TABLET;ORAL	125MG	GRISEOFULVIN, ULTRAMICROSIZE	1975-04-16	Prescription	No
050475	NDA	BAUSCH	002	GRIS-PEG	TABLET;ORAL	250MG	GRISEOFULVIN, ULTRAMICROSIZE	1975-04-16	Prescription	No
083976	ANDA	BAUSCH	001	TESTRED	CAPSULE;ORAL	10MG	METHYLTESTOSTERONE	1973-12-03	Discontinued	No
050445	NDA	BAUSCH	001	MINOCIN	SUSPENSION;ORAL	EQ 50MG BASE/5ML	MINOCYCLINE HYDROCHLORIDE	1972-10-26	Discontinued	No
080442	ANDA	BAUSCH	002	NUTRACORT	CREAM;TOPICAL	0.5%	HYDROCORTISONE	1972-04-04	Discontinued	No
080442	ANDA	BAUSCH	003	NUTRACORT	CREAM;TOPICAL	1%	HYDROCORTISONE	1972-04-04	Discontinued	No
080426	ANDA	BAUSCH	001	CETACORT	LOTION;TOPICAL	1%	HYDROCORTISONE	1971-12-22	Discontinued	No
080426	ANDA	BAUSCH	002	CETACORT	LOTION;TOPICAL	0.5%	HYDROCORTISONE	1971-12-22	Discontinued	No
017001	NDA	BAUSCH	001	ANCOBON	CAPSULE;ORAL	250MG	FLUCYTOSINE	1971-11-26	Prescription	No
017001	NDA	BAUSCH	002	ANCOBON	CAPSULE;ORAL	500MG	FLUCYTOSINE	1971-11-26	Prescription	Yes
016092	NDA	BAUSCH	001	EDECRIN	TABLET;ORAL	25MG	ETHACRYNIC ACID	1967-01-10	Prescription	Yes
016092	NDA	BAUSCH	002	EDECRIN	TABLET;ORAL	50MG	ETHACRYNIC ACID	1967-01-10	Discontinued	No
016093	NDA	BAUSCH	001	EDECRIN	INJECTABLE;INJECTION	EQ 50MG BASE/VIAL	ETHACRYNATE SODIUM	1967-01-10	Prescription	Yes
012750	NDA	BAUSCH	001	LIBRAX	CAPSULE;ORAL	5MG;2.5MG	CHLORDIAZEPOXIDE HYDROCHLORIDE; CLIDINIUM BROMIDE	1966-09-01	Prescription	Yes
015193	NDA	BAUSCH	001	MESTINON	SYRUP;ORAL	60MG/5ML	PYRIDOSTIGMINE BROMIDE	1965-01-25	Prescription	Yes
013416	NDA	BAUSCH	003	NORGESIC	TABLET;ORAL	385MG;30MG;25MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ASPIRIN; CAFFEINE; ORPHENADRINE CITRATE	1964-03-04	Discontinued	No
013416	NDA	BAUSCH	004	NORGESIC FORTE	TABLET;ORAL	770MG;60MG;50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ASPIRIN; CAFFEINE; ORPHENADRINE CITRATE	1964-03-04	Discontinued	No
012301	NDA	BAUSCH	001	LIBRIUM	INJECTABLE;INJECTION	100MG/AMP	CHLORDIAZEPOXIDE HYDROCHLORIDE	1961-07-21	Discontinued	No
012093	NDA	BAUSCH	001	ISORDIL	TABLET;ORAL	40MG	ISOSORBIDE DINITRATE	1959-11-09	Prescription	Yes
			002	ISORDIL	TABLET;ORAL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ISOSORBIDE DINITRATE	1959-11-09	Discontinued	No
			005	ISORDIL	TABLET;ORAL	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ISOSORBIDE DINITRATE	1959-11-09	Discontinued	No
			006	ISORDIL	TABLET;ORAL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ISOSORBIDE DINITRATE	1959-11-09	Discontinued	No
			007	ISORDIL	TABLET;ORAL	5MG	ISOSORBIDE DINITRATE	1959-11-09	Prescription	No
012157	NDA	BAUSCH	001	NORFLEX	TABLET, EXTENDED RELEASE;ORAL	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ORPHENADRINE CITRATE	1959-11-04	Discontinued	No
011665	NDA	BAUSCH	001	MESTINON	TABLET, EXTENDED RELEASE;ORAL	180MG	PYRIDOSTIGMINE BROMIDE	1959-01-12	Prescription	Yes
010515	NDA	BAUSCH	001	ISUPREL	INJECTABLE;INJECTION	0.2MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ISOPROTERENOL HYDROCHLORIDE	1956-05-25	Discontinued	No
009830	NDA	BAUSCH	001	MESTINON	INJECTABLE;INJECTION	5MG/ML	PYRIDOSTIGMINE BROMIDE	1955-10-02	Prescription	Yes
010104	NDA	BAUSCH	003	MEPHYTON	TABLET;ORAL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	PHYTONADIONE	1955-09-30	Discontinued	No
009829	NDA	BAUSCH	002	MESTINON	TABLET;ORAL	60MG	PYRIDOSTIGMINE BROMIDE	1955-04-06	Prescription	Yes
008922	NDA	BAUSCH	001	CALCIUM DISODIUM VERSENATE	INJECTABLE;INJECTION	200MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	EDETATE CALCIUM DISODIUM	1953-07-16	Discontinued	No
008922	NDA	BAUSCH	002	CALCIUM DISODIUM VERSENATE	TABLET;ORAL	500MG	EDETATE CALCIUM DISODIUM	1953-07-16	Discontinued	No
005929	NDA	BAUSCH	001	D.H.E. 45	INJECTABLE;INJECTION	1MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DIHYDROERGOTAMINE MESYLATE	1946-04-12	Discontinued	No