FDA Approved Products

Application #	Type	Sponsor	Product #	Drug Name	Form	Strength	Active Ingredient	Approval Date	Marketing Status	Reference Standard
761325	BLA	SANOFI-AVENTIS U.S. LLC	001	MERILOG	INJECTION;SOLUTION	10ML(100UNITS/ML)	INSULIN ASPART-SZJJ	2025-02-14	Prescription	No
761325	BLA	SANOFI-AVENTIS U.S. LLC	002	MERILOG SOLOSTAR	INJECTION;SOLUTION	3ML(100UNITS/ML)	INSULIN ASPART-SZJJ	2025-02-14	Prescription	No
214429	NDA	SANOFI	001	FEXINIDAZOLE	TABLET;ORAL	600MG	FEXINIDAZOLE	2021-07-16	Prescription	Yes
761113	BLA	SANOFI AVENTIS US	001	SARCLISA	INJECTABLE;INJECTION	100MG/5ML (20MG/ML)	ISATUXIMAB-IRFC	2020-03-02	Prescription	No
761113	BLA	SANOFI AVENTIS US	002	SARCLISA	INJECTABLE;INJECTION	500MG/25ML (20MG/ML)	ISATUXIMAB-IRFC	2020-03-02	Prescription	No
209196	BLA	SANOFI-AVENTIS US	001	ADMELOG	SOLUTION;INTRAVENOUS, SUBCUTANEOUS	1000 UNITS/10ML (100 UNITS/ML)	INSULIN LISPRO	2017-12-11	Prescription	No
			003	ADMELOG	SOLUTION;INTRAVENOUS, SUBCUTANEOUS	300 UNITS/3ML (100 UNITS/ML)	INSULIN LISPRO	2017-12-11	Prescription	No
			002	ADMELOG SOLOSTAR	SOLUTION;INTRAVENOUS, SUBCUTANEOUS	300 UNITS/3ML (100 UNITS/ML)	INSULIN LISPRO	2017-12-11	Prescription	No
761037	BLA	SANOFI SYNTHELABO	001	KEVZARA	INJECTABLE;INJECTION	150MG/1.14ML	SARILUMAB	2017-05-22	Prescription	No
761037	BLA	SANOFI SYNTHELABO	002	KEVZARA	INJECTABLE;INJECTION	200MG/1.14ML	SARILUMAB	2017-05-22	Prescription	No
209089	NDA	CHATTEM SANOFI	001	XYZAL ALLERGY 24HR	TABLET;ORAL	5MG	LEVOCETIRIZINE DIHYDROCHLORIDE	2017-01-31	Over-the-counter	Yes
209090	NDA	CHATTEM SANOFI	001	XYZAL ALLERGY 24HR	SOLUTION;ORAL	2.5MG/5ML	LEVOCETIRIZINE DIHYDROCHLORIDE	2017-01-31	Over-the-counter	Yes
208673	BLA	SANOFI-AVENTIS US	001	SOLIQUA 100/33	SOLUTION;SUBCUTANEOUS	300 UNITS/3ML;99MCG/3ML (100 UNITS/ML;33MCG/ML)	INSULIN GLARGINE; LIXISENATIDE	2016-11-21	Prescription	No
208471	BLA	SANOFI-AVENTIS US	001	ADLYXIN	SOLUTION;SUBCUTANEOUS	0.15MG/3ML (0.05MG/ML)	LIXISENATIDE	2016-07-27	Prescription	No
208471	BLA	SANOFI-AVENTIS US	002	ADLYXIN	SOLUTION;SUBCUTANEOUS	0.3MG/3ML (0.1MG/ML)	LIXISENATIDE	2016-07-27	Prescription	No
206538	BLA	SANOFI US SERVICES	002	TOUJEO MAX SOLOSTAR	SOLUTION;SUBCUTANEOUS	900 UNITS/3ML (300 UNITS/ML)	INSULIN GLARGINE RECOMBINANT	2015-02-25	Prescription	No
206538	BLA	SANOFI US SERVICES	001	TOUJEO SOLOSTAR	SOLUTION;SUBCUTANEOUS	450 UNITS/1.5ML (300 UNITS/ML)	INSULIN GLARGINE RECOMBINANT	2015-02-25	Prescription	No
202992	NDA	SANOFI AVENTIS US	001	AUBAGIO	TABLET;ORAL	7MG	TERIFLUNOMIDE	2012-09-12	Prescription	No
202992	NDA	SANOFI AVENTIS US	002	AUBAGIO	TABLET;ORAL	14MG	TERIFLUNOMIDE	2012-09-12	Prescription	Yes
125418	BLA	SANOFI AVENTIS US	001	ZALTRAP	INJECTABLE; INJECTION	4MG	ZIV-AFLIBERCEPT	2012-08-03	Prescription	No
201373	NDA	CHATTEM SANOFI	001	CHILDREN'S ALLEGRA ALLERGY	SUSPENSION;ORAL	30MG/5ML	FEXOFENADINE HYDROCHLORIDE	2011-01-24	Over-the-counter	Yes
201373	NDA	CHATTEM SANOFI	002	CHILDREN'S ALLEGRA HIVES	SUSPENSION;ORAL	30MG/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	FEXOFENADINE HYDROCHLORIDE	2011-01-24	Discontinued	No
201023	NDA	SANOFI AVENTIS US	001	JEVTANA KIT	SOLUTION;INTRAVENOUS	60MG/1.5ML (40MG/ML)	CABAZITAXEL	2010-06-17	Prescription	Yes
022425	NDA	SANOFI AVENTIS US	001	MULTAQ	TABLET;ORAL	EQ 400MG BASE	DRONEDARONE HYDROCHLORIDE	2009-07-01	Prescription	Yes
022273	NDA	SANOFI AVENTIS US	001	OFORTA	TABLET;ORAL	10MG	FLUDARABINE PHOSPHATE	2008-12-18	Discontinued	No
022157	NDA	CHATTEM SANOFI	001	XYZAL	SOLUTION;ORAL	2.5MG/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	LEVOCETIRIZINE DIHYDROCHLORIDE	2008-01-28	Discontinued	No
022127	NDA	SANOFI	001	RENVELA	TABLET;ORAL	800MG	SEVELAMER CARBONATE	2007-10-19	Prescription	Yes
021909	NDA	CHATTEM SANOFI	002	CHILDREN'S ALLEGRA ALLERGY	TABLET, ORALLY DISINTEGRATING;ORAL	30MG	FEXOFENADINE HYDROCHLORIDE	2007-07-26	Discontinued	No
021909	NDA	CHATTEM SANOFI	003	CHILDREN'S ALLEGRA HIVES	TABLET, ORALLY DISINTEGRATING;ORAL	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	FEXOFENADINE HYDROCHLORIDE	2007-07-26	Discontinued	No
022064	NDA	CHATTEM SANOFI	001	XYZAL	TABLET;ORAL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	LEVOCETIRIZINE DIHYDROCHLORIDE	2007-05-25	Discontinued	No
022138	NDA	SANOFI AVENTIS US	001	LOVENOX	INJECTABLE; INJECTION	100MG/ML	ENOXAPARIN SODIUM	2007-05-16	Prescription	No
021963	NDA	CHATTEM SANOFI	001	ALLEGRA	SUSPENSION;ORAL	30MG/5ML	FEXOFENADINE HYDROCHLORIDE	2006-10-16	Discontinued	No
021759	NDA	SANOFI AVENTIS US	001	ELOXATIN	INJECTABLE;INTRAVENOUS	50MG/10ML (5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	OXALIPLATIN	2005-01-31	Discontinued	No
			002	ELOXATIN	INJECTABLE;INTRAVENOUS	100MG/20ML (5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	OXALIPLATIN	2005-01-31	Discontinued	No
			003	ELOXATIN	INJECTABLE;INTRAVENOUS	200MG/40ML (5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	OXALIPLATIN	2005-01-31	Discontinued	No
021704	NDA	CHATTEM SANOFI	002	ALLEGRA-D 24 HOUR ALLERGY AND CONGESTION	TABLET, EXTENDED RELEASE;ORAL	180MG;240MG	FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE	2004-10-19	Over-the-counter	Yes
021698	NDA	CHATTEM SANOFI	001	ZANTAC 150	TABLET;ORAL	EQ 150MG BASE	RANITIDINE HYDROCHLORIDE	2004-08-31	Discontinued	No
021698	NDA	CHATTEM SANOFI	002	ZANTAC 150	TABLET;ORAL	EQ 150MG BASE	RANITIDINE HYDROCHLORIDE	2004-08-31	Discontinued	No
021629	BLA	SANOFI AVENTIS US	001	APIDRA	INJECTABLE;INTRAVENOUS, SUBCUTANEOUS	1000 UNITS/10ML (100 UNITS/ML)	INSULIN GLULISINE RECOMBINANT	2004-04-16	Prescription	No
			002	APIDRA	INJECTABLE;INTRAVENOUS, SUBCUTANEOUS	300 UNITS/3ML (100 UNITS/ML)	INSULIN GLULISINE RECOMBINANT	2004-04-16	Discontinued	No
			003	APIDRA SOLOSTAR	INJECTABLE;SUBCUTANEOUS	300 UNITS/3ML	INSULIN GLULISINE RECOMBINANT	2004-04-16	Prescription	No
020784	NDA	SANOFI AVENTIS US	001	NASACORT HFA	SPRAY, METERED;NASAL	0.055MG/SPRAY	TRIAMCINOLONE ACETONIDE	2004-04-07	Discontinued	No
021144	NDA	SANOFI AVENTIS US	001	KETEK	TABLET;ORAL	400MG	TELITHROMYCIN	2004-04-01	Discontinued	No
021144	NDA	SANOFI AVENTIS US	002	KETEK	TABLET;ORAL	300MG	TELITHROMYCIN	2004-04-01	Discontinued	No
021492	NDA	SANOFI AVENTIS US	001	ELOXATIN	INJECTABLE;INTRAVENOUS	50MG/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	OXALIPLATIN	2002-08-09	Discontinued	No
021492	NDA	SANOFI AVENTIS US	002	ELOXATIN	INJECTABLE;INTRAVENOUS	100MG/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	OXALIPLATIN	2002-08-09	Discontinued	No
103946	BLA	SANOFI SYNTHELABO	001	ELITEK	VIAL; INTRAVENOUS	1.5MG/VIAL	RASBURICASE	2002-07-12	Prescription	No
021081	BLA	SANOFI AVENTIS US	001	LANTUS	INJECTABLE;INJECTION	100 UNITS/ML	INSULIN GLARGINE RECOMBINANT	2000-04-20	Prescription	Yes
021081	BLA	SANOFI AVENTIS US	002	LANTUS SOLOSTAR	INJECTABLE;INJECTION	300 UNITS/3ML (100 UNITS/ML)	INSULIN GLARGINE RECOMBINANT	2000-04-20	Prescription	Yes
021027	NDA	SANOFI	001	HECTOROL	INJECTABLE;INJECTION	4MCG/2ML (2MCG/ML)	DOXERCALCIFEROL	2000-04-06	Prescription	Yes
021027	NDA	SANOFI	002	HECTOROL	INJECTABLE;INJECTION	2MCG/ML (2MCG/ML)	DOXERCALCIFEROL	2000-04-06	Prescription	No
020872	NDA	CHATTEM SANOFI	007	ALLEGRA ALLERGY	TABLET;ORAL	60MG	FEXOFENADINE HYDROCHLORIDE	2000-02-25	Over-the-counter	No
			010	ALLEGRA ALLERGY	TABLET;ORAL	180MG	FEXOFENADINE HYDROCHLORIDE	2000-02-25	Over-the-counter	Yes
			008	ALLEGRA HIVES	TABLET;ORAL	60MG	FEXOFENADINE HYDROCHLORIDE	2000-02-25	Discontinued	No
			009	ALLEGRA HIVES	TABLET;ORAL	180MG	FEXOFENADINE HYDROCHLORIDE	2000-02-25	Over-the-counter	Yes
			005	CHILDREN'S ALLEGRA ALLERGY	TABLET;ORAL	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	FEXOFENADINE HYDROCHLORIDE	2000-02-25	Discontinued	No
			006	CHILDREN'S ALLEGRA HIVES	TABLET;ORAL	30MG	FEXOFENADINE HYDROCHLORIDE	2000-02-25	Discontinued	No
020862	NDA	SANOFI	001	HECTOROL	CAPSULE;ORAL	2.5MCG	DOXERCALCIFEROL	1999-06-09	Discontinued	No
			002	HECTOROL	CAPSULE;ORAL	0.5MCG	DOXERCALCIFEROL	1999-06-09	Discontinued	No
			003	HECTOROL	CAPSULE;ORAL	1MCG	DOXERCALCIFEROL	1999-06-09	Discontinued	No
020955	NDA	SANOFI AVENTIS US	001	FERRLECIT	INJECTABLE;INJECTION	EQ 62.5MG IRON/5ML (EQ 12.5MG IRON/ML)	SODIUM FERRIC GLUCONATE COMPLEX	1999-02-18	Prescription	Yes
020905	NDA	SANOFI AVENTIS US	001	ARAVA	TABLET;ORAL	10MG	LEFLUNOMIDE	1998-09-10	Prescription	No
			002	ARAVA	TABLET;ORAL	20MG	LEFLUNOMIDE	1998-09-10	Prescription	Yes
			003	ARAVA	TABLET;ORAL	100MG	LEFLUNOMIDE	1998-09-10	Prescription	Yes
021024	NDA	SANOFI AVENTIS US	001	PRIFTIN	TABLET;ORAL	150MG	RIFAPENTINE	1998-06-22	Prescription	Yes
020745	NDA	CHATTEM SANOFI	001	ZANTAC 75	TABLET, EFFERVESCENT;ORAL	EQ 75MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	RANITIDINE HYDROCHLORIDE	1998-02-26	Discontinued	No
020786	NDA	CHATTEM SANOFI	002	ALLEGRA-D 12 HOUR ALLERGY AND CONGESTION	TABLET, EXTENDED RELEASE;ORAL	60MG;120MG	FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE	1997-12-24	Over-the-counter	Yes
020839	NDA	SANOFI AVENTIS US	001	PLAVIX	TABLET;ORAL	EQ 75MG BASE	CLOPIDOGREL BISULFATE	1997-11-17	Prescription	No
020839	NDA	SANOFI AVENTIS US	002	PLAVIX	TABLET;ORAL	EQ 300MG BASE	CLOPIDOGREL BISULFATE	1997-11-17	Prescription	No
020750	NDA	SANOFI AVENTIS US	001	TILADE	SOLUTION;INHALATION	0.5%	NEDOCROMIL SODIUM	1997-10-01	Discontinued	No
020758	NDA	SANOFI AVENTIS US	001	AVALIDE	TABLET;ORAL	12.5MG;75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	HYDROCHLOROTHIAZIDE; IRBESARTAN	1997-09-30	Discontinued	No
			002	AVALIDE	TABLET;ORAL	12.5MG;150MG	HYDROCHLOROTHIAZIDE; IRBESARTAN	1997-09-30	Prescription	Yes
			003	AVALIDE	TABLET;ORAL	12.5MG;300MG	HYDROCHLOROTHIAZIDE; IRBESARTAN	1997-09-30	Prescription	Yes
			004	AVALIDE	TABLET;ORAL	25MG;300MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	HYDROCHLOROTHIAZIDE; IRBESARTAN	1997-09-30	Discontinued	No
020757	NDA	SANOFI AVENTIS US	001	AVAPRO	TABLET;ORAL	75MG	IRBESARTAN	1997-09-30	Discontinued	No
			002	AVAPRO	TABLET;ORAL	150MG	IRBESARTAN	1997-09-30	Prescription	No
			003	AVAPRO	TABLET;ORAL	300MG	IRBESARTAN	1997-09-30	Prescription	Yes
020579	NDA	SANOFI	001	FLOMAX	CAPSULE;ORAL	0.4MG	TAMSULOSIN HYDROCHLORIDE	1997-04-15	Discontinued	No
020707	NDA	SANOFI AVENTIS US	001	SKELID	TABLET;ORAL	EQ 200MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TILUDRONATE DISODIUM	1997-03-07	Discontinued	No
020625	NDA	CHATTEM SANOFI	001	ALLEGRA	CAPSULE;ORAL	60MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	FEXOFENADINE HYDROCHLORIDE	1996-07-25	Discontinued	No
020468	NDA	CHATTEM SANOFI	002	NASACORT ALLERGY 24 HOUR	SPRAY, METERED;NASAL	0.055MG/SPRAY	TRIAMCINOLONE ACETONIDE	1996-05-20	Over-the-counter	Yes
020449	NDA	SANOFI AVENTIS US	001	TAXOTERE	INJECTABLE;INJECTION	40MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DOCETAXEL	1996-05-14	Discontinued	No
			003	TAXOTERE	INJECTABLE;INJECTION	20MG/ML (20MG/ML)	DOCETAXEL	1996-05-14	Discontinued	No
			004	TAXOTERE	INJECTABLE;INJECTION	80MG/4ML (20MG/ML)	DOCETAXEL	1996-05-14	Discontinued	No
			005	TAXOTERE	INJECTABLE;INJECTION	160MG/8ML (20MG/ML)	DOCETAXEL	1996-05-14	Prescription	No
020520	NDA	CHATTEM SANOFI	001	ZANTAC 75	TABLET;ORAL	EQ 75MG BASE	RANITIDINE HYDROCHLORIDE	1995-12-19	Discontinued	No
020496	NDA	SANOFI AVENTIS US	001	AMARYL	TABLET;ORAL	1MG	GLIMEPIRIDE	1995-11-30	Discontinued	No
			002	AMARYL	TABLET;ORAL	2MG	GLIMEPIRIDE	1995-11-30	Discontinued	No
			003	AMARYL	TABLET;ORAL	4MG	GLIMEPIRIDE	1995-11-30	Discontinued	No
020343	NDA	SANOFI AVENTIS US	001	PRIMACOR IN DEXTROSE 5% IN PLASTIC CONTAINER	INJECTABLE;INJECTION	EQ 10MG BASE/100ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MILRINONE LACTATE	1994-08-09	Discontinued	No
			002	PRIMACOR IN DEXTROSE 5% IN PLASTIC CONTAINER	INJECTABLE;INJECTION	EQ 15MG BASE/100ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MILRINONE LACTATE	1994-08-09	Discontinued	No
			003	PRIMACOR IN DEXTROSE 5% IN PLASTIC CONTAINER	INJECTABLE;INJECTION	EQ 20MG BASE/100ML (EQ 0.2MG BASE/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MILRINONE LACTATE	1994-08-09	Discontinued	No
			004	PRIMACOR IN DEXTROSE 5% IN PLASTIC CONTAINER	INJECTABLE;INJECTION	EQ 40MG BASE/200ML (EQ 0.2MG BASE/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MILRINONE LACTATE	1994-08-09	Discontinued	No
050705	NDA	SANOFI AVENTIS US	001	RIFATER	TABLET;ORAL	50MG;300MG;120MG	ISONIAZID; PYRAZINAMIDE; RIFAMPIN	1994-05-31	Discontinued	No
020164	NDA	SANOFI AVENTIS US	009	LOVENOX	INJECTABLE;INTRAVENOUS, SUBCUTANEOUS	300MG/3ML (100MG/ML)	ENOXAPARIN SODIUM	1993-03-29	Prescription	No
			001	LOVENOX (PRESERVATIVE FREE)	INJECTABLE;SUBCUTANEOUS	30MG/0.3ML (100MG/ML)	ENOXAPARIN SODIUM	1993-03-29	Prescription	No
			002	LOVENOX (PRESERVATIVE FREE)	INJECTABLE;SUBCUTANEOUS	40MG/0.4ML (100MG/ML)	ENOXAPARIN SODIUM	1993-03-29	Prescription	No
			003	LOVENOX (PRESERVATIVE FREE)	INJECTABLE;SUBCUTANEOUS	60MG/0.6ML (100MG/ML)	ENOXAPARIN SODIUM	1993-03-29	Prescription	No
			004	LOVENOX (PRESERVATIVE FREE)	INJECTABLE;SUBCUTANEOUS	80MG/0.8ML (100MG/ML)	ENOXAPARIN SODIUM	1993-03-29	Prescription	No
			005	LOVENOX (PRESERVATIVE FREE)	INJECTABLE;SUBCUTANEOUS	100MG/ML (100MG/ML)	ENOXAPARIN SODIUM	1993-03-29	Prescription	Yes
			006	LOVENOX (PRESERVATIVE FREE)	INJECTABLE;SUBCUTANEOUS	90MG/0.6ML (150MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ENOXAPARIN SODIUM	1993-03-29	Discontinued	No
			007	LOVENOX (PRESERVATIVE FREE)	INJECTABLE;SUBCUTANEOUS	120MG/0.8ML (150MG/ML)	ENOXAPARIN SODIUM	1993-03-29	Prescription	No
			008	LOVENOX (PRESERVATIVE FREE)	INJECTABLE;SUBCUTANEOUS	150MG/ML (150MG/ML)	ENOXAPARIN SODIUM	1993-03-29	Prescription	No
019807	NDA	SANOFI AVENTIS US	001	KERLEDEX	TABLET;ORAL	5MG;12.5MG	BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE	1992-10-30	Discontinued	No
019807	NDA	SANOFI AVENTIS US	002	KERLEDEX	TABLET;ORAL	10MG;12.5MG	BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE	1992-10-30	Discontinued	No
020055	NDA	SANOFI AVENTIS US	001	GLYBURIDE (MICRONIZED)	TABLET;ORAL	1.5MG	GLYBURIDE	1992-04-17	Discontinued	No
			002	GLYBURIDE (MICRONIZED)	TABLET;ORAL	3MG	GLYBURIDE	1992-04-17	Discontinued	No
			003	GLYBURIDE (MICRONIZED)	TABLET;ORAL	6MG	GLYBURIDE	1992-04-17	Discontinued	No
019548	NDA	SANOFI AVENTIS US	001	TORNALATE	SOLUTION;INHALATION	0.2%	BITOLTEROL MESYLATE	1992-02-19	Discontinued	No
019616	NDA	SANOFI AVENTIS US	004	PENETREX	TABLET;ORAL	200MG	ENOXACIN	1991-12-31	Discontinued	No
019616	NDA	SANOFI AVENTIS US	005	PENETREX	TABLET;ORAL	400MG	ENOXACIN	1991-12-31	Discontinued	No
020165	NDA	CHATTEM SANOFI	004	NICODERM CQ	FILM, EXTENDED RELEASE;TRANSDERMAL	21MG/24HR	NICOTINE	1991-11-07	Over-the-counter	Yes
			005	NICODERM CQ	FILM, EXTENDED RELEASE;TRANSDERMAL	14MG/24HR	NICOTINE	1991-11-07	Over-the-counter	No
			006	NICODERM CQ	FILM, EXTENDED RELEASE;TRANSDERMAL	7MG/24HR	NICOTINE	1991-11-07	Over-the-counter	No
019798	NDA	CHATTEM SANOFI	001	NASACORT	AEROSOL, METERED;NASAL	0.055MG/INH	TRIAMCINOLONE ACETONIDE	1991-07-11	Discontinued	No
019879	NDA	SANOFI AVENTIS US	002	ORNIDYL	INJECTABLE;INJECTION	200MG/ML	EFLORNITHINE HYDROCHLORIDE	1990-11-28	Discontinued	No
071159	ANDA	SANOFI AVENTIS US	001	NITRO-BID	INJECTABLE;INJECTION	10MG/ML	NITROGLYCERIN	1990-02-28	Discontinued	No
019507	NDA	SANOFI AVENTIS US	001	KERLONE	TABLET;ORAL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	BETAXOLOL HYDROCHLORIDE	1989-10-27	Discontinued	No
019507	NDA	SANOFI AVENTIS US	002	KERLONE	TABLET;ORAL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	BETAXOLOL HYDROCHLORIDE	1989-10-27	Discontinued	No
050627	NDA	SANOFI AVENTIS US	001	RIFADIN	INJECTABLE;INJECTION	600MG/VIAL	RIFAMPIN	1989-05-25	Prescription	Yes
089539	ANDA	SANOFI AVENTIS US	001	SLO-BID	CAPSULE, EXTENDED RELEASE;ORAL	75MG	THEOPHYLLINE	1989-05-10	Discontinued	No
089540	ANDA	SANOFI AVENTIS US	001	SLO-BID	CAPSULE, EXTENDED RELEASE;ORAL	125MG	THEOPHYLLINE	1989-05-10	Discontinued	No
019436	NDA	SANOFI AVENTIS US	001	PRIMACOR	INJECTABLE;INJECTION	EQ 1MG BASE/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	MILRINONE LACTATE	1987-12-31	Discontinued	No
062659	ANDA	SANOFI AVENTIS US	001	CLAFORAN	INJECTABLE;INJECTION	EQ 1GM BASE/VIAL	CEFOTAXIME SODIUM	1987-01-13	Discontinued	No
062659	ANDA	SANOFI AVENTIS US	002	CLAFORAN	INJECTABLE;INJECTION	EQ 2GM BASE/VIAL	CEFOTAXIME SODIUM	1987-01-13	Discontinued	No
018000	NDA	SANOFI AVENTIS US	001	BRICANYL	AEROSOL, METERED;INHALATION	0.2MG/INH	TERBUTALINE SULFATE	1985-03-19	Discontinued	No
087892	ANDA	SANOFI AVENTIS US	001	SLO-BID	CAPSULE, EXTENDED RELEASE;ORAL	100MG	THEOPHYLLINE	1985-01-31	Discontinued	No
087893	ANDA	SANOFI AVENTIS US	001	SLO-BID	CAPSULE, EXTENDED RELEASE;ORAL	200MG	THEOPHYLLINE	1985-01-31	Discontinued	No
087894	ANDA	SANOFI AVENTIS US	001	SLO-BID	CAPSULE, EXTENDED RELEASE;ORAL	300MG	THEOPHYLLINE	1985-01-31	Discontinued	No
088269	ANDA	SANOFI AVENTIS US	001	SLO-BID	CAPSULE, EXTENDED RELEASE;ORAL	50MG	THEOPHYLLINE	1985-01-31	Discontinued	No
018770	NDA	SANOFI AVENTIS US	001	TORNALATE	AEROSOL, METERED;INHALATION	0.37MG/INH	BITOLTEROL MESYLATE	1984-12-28	Discontinued	No
018700	NDA	SANOFI AVENTIS US	001	INOCOR	INJECTABLE;INJECTION	EQ 5MG BASE/ML	INAMRINONE LACTATE	1984-07-31	Discontinued	No
017532	NDA	SANOFI AVENTIS US	001	DIABETA	TABLET;ORAL	1.25MG	GLYBURIDE	1984-05-01	Prescription	No
			002	DIABETA	TABLET;ORAL	2.5MG	GLYBURIDE	1984-05-01	Prescription	No
			003	DIABETA	TABLET;ORAL	5MG	GLYBURIDE	1984-05-01	Prescription	Yes
018685	NDA	CHATTEM SANOFI	001	GAVISCON	TABLET, CHEWABLE;ORAL	80MG;20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE	1983-12-09	Discontinued	No
018685	NDA	CHATTEM SANOFI	002	GAVISCON	TABLET, CHEWABLE;ORAL	160MG;40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE	1983-12-09	Discontinued	No
018538	NDA	SANOFI AVENTIS US	001	LOZOL	TABLET;ORAL	2.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INDAPAMIDE	1983-07-06	Discontinued	No
018538	NDA	SANOFI AVENTIS US	002	LOZOL	TABLET;ORAL	1.25MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INDAPAMIDE	1983-07-06	Discontinued	No
018733	NDA	SANOFI AVENTIS US	001	TALWIN NX	TABLET;ORAL	EQ 0.5MG BASE;EQ 50MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	NALOXONE HYDROCHLORIDE; PENTAZOCINE HYDROCHLORIDE	1982-12-16	Discontinued	No
018458	NDA	SANOFI AVENTIS US	001	TALACEN	TABLET;ORAL	650MG;EQ 25MG BASE	ACETAMINOPHEN; PENTAZOCINE HYDROCHLORIDE	1982-09-23	Discontinued	No
018621	NDA	SANOFI AVENTIS US	001	NITRO-BID	INJECTABLE;INJECTION	5MG/ML	NITROGLYCERIN	1982-01-05	Discontinued	No
087260	ANDA	SANOFI AVENTIS US	001	AZOLID	CAPSULE;ORAL	100MG	PHENYLBUTAZONE	1981-10-13	Discontinued	No
061876	ANDA	SANOFI AVENTIS US	001	CERUBIDINE	INJECTABLE;INJECTION	EQ 20MG BASE/VIAL	DAUNORUBICIN HYDROCHLORIDE	1980-02-05	Discontinued	No
085202	ANDA	SANOFI AVENTIS US	001	SLO-PHYLLIN	TABLET;ORAL	100MG	THEOPHYLLINE	1979-11-14	Discontinued	No
085204	ANDA	SANOFI AVENTIS US	001	SLO-PHYLLIN	TABLET;ORAL	200MG	THEOPHYLLINE	1979-11-14	Discontinued	No
017884	NDA	SANOFI AVENTIS US	001	CHRONULAC	SOLUTION;ORAL	10GM/15ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	LACTULOSE	1979-06-20	Discontinued	No
085187	ANDA	SANOFI AVENTIS US	001	SLO-PHYLLIN	SYRUP;ORAL	80MG/15ML	THEOPHYLLINE	1979-05-15	Discontinued	No
017769	NDA	SANOFI AVENTIS US	001	CALCIMAR	INJECTABLE;INJECTION	200 IU/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CALCITONIN SALMON	1978-04-17	Discontinued	No
017446	NDA	SANOFI AVENTIS US	001	PHISO-SCRUB	SPONGE;TOPICAL	3%	HEXACHLOROPHENE	1977-08-01	Discontinued	No
017688	NDA	SANOFI AVENTIS US	001	LASIX	SOLUTION;ORAL	10MG/ML	FUROSEMIDE	1977-03-08	Discontinued	No
017535	NDA	SANOFI AVENTIS US	001	LORELCO	TABLET;ORAL	250MG	PROBUCOL	1977-02-01	Discontinued	No
017535	NDA	SANOFI AVENTIS US	002	LORELCO	TABLET;ORAL	500MG	PROBUCOL	1977-02-01	Discontinued	No
017557	NDA	SANOFI AVENTIS US	002	DANOCRINE	CAPSULE;ORAL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DANAZOL	1976-06-21	Discontinued	No
			003	DANOCRINE	CAPSULE;ORAL	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DANAZOL	1976-06-21	Discontinued	No
			004	DANOCRINE	CAPSULE;ORAL	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DANAZOL	1976-06-21	Discontinued	No
017657	NDA	SANOFI AVENTIS US	001	CEPHULAC	SOLUTION;ORAL, RECTAL	10GM/15ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	LACTULOSE	1976-03-25	Discontinued	No
016891	NDA	SANOFI AVENTIS US	001	TALWIN COMPOUND	TABLET;ORAL	325MG;EQ 12.5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ASPIRIN; PENTAZOCINE HYDROCHLORIDE	1975-11-12	Discontinued	No
017603	NDA	SANOFI AVENTIS US	001	NOVAFED	CAPSULE, EXTENDED RELEASE;ORAL	120MG	PSEUDOEPHEDRINE HYDROCHLORIDE	1975-08-29	Discontinued	No
061884	ANDA	SANOFI AVENTIS US	001	RIFAMATE	CAPSULE;ORAL	150MG;300MG	ISONIAZID; RIFAMPIN	1975-07-11	Discontinued	No
017618	NDA	SANOFI AVENTIS US	001	BRICANYL	TABLET;ORAL	2.5MG	TERBUTALINE SULFATE	1975-04-22	Discontinued	No
017618	NDA	SANOFI AVENTIS US	002	BRICANYL	TABLET;ORAL	5MG	TERBUTALINE SULFATE	1975-04-22	Discontinued	No
017668	NDA	SANOFI AVENTIS US	001	TENUATE	TABLET;ORAL	25MG	DIETHYLPROPION HYDROCHLORIDE	1975-03-20	Discontinued	No
017669	NDA	SANOFI AVENTIS US	001	TENUATE	TABLET, EXTENDED RELEASE;ORAL	75MG	DIETHYLPROPION HYDROCHLORIDE	1975-03-20	Discontinued	No
017466	NDA	SANOFI AVENTIS US	001	BRICANYL	INJECTABLE;INJECTION	1MG/ML	TERBUTALINE SULFATE	1974-03-25	Discontinued	No
083823	ANDA	SANOFI AVENTIS US	001	NICOLAR	TABLET;ORAL	500MG	NIACIN	1973-11-26	Discontinued	No
017430	NDA	SANOFI AVENTIS US	001	NEGGRAM	SUSPENSION;ORAL	250MG/5ML	NALIDIXIC ACID	1973-04-17	Discontinued	No
050420	NDA	SANOFI AVENTIS US	001	RIFADIN	CAPSULE;ORAL	300MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	RIFAMPIN	1971-05-21	Discontinued	No
050420	NDA	SANOFI AVENTIS US	002	RIFADIN	CAPSULE;ORAL	150MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	RIFAMPIN	1971-05-21	Discontinued	No
088746	ANDA	SANOFI AVENTIS US	001	ACCURBRON	SYRUP;ORAL	150MG/15ML	THEOPHYLLINE		Discontinued	No
087091	ANDA	SANOFI AVENTIS US	001	AZOLID	TABLET;ORAL	100MG	PHENYLBUTAZONE		Discontinued	No
085264	ANDA	SANOFI AVENTIS US	001	BRONKODYL	CAPSULE;ORAL	100MG	THEOPHYLLINE		Discontinued	No
085264	ANDA	SANOFI AVENTIS US	002	BRONKODYL	CAPSULE;ORAL	200MG	THEOPHYLLINE		Discontinued	No
012339	NDA	SANOFI AVENTIS US	007	BRONKOMETER	AEROSOL, METERED;INHALATION	0.34MG/INH	ISOETHARINE MESYLATE		Discontinued	No
			008	BRONKOSOL	SOLUTION;INHALATION	1%	ISOETHARINE HYDROCHLORIDE		Discontinued	No
			009	BRONKOSOL	SOLUTION;INHALATION	0.25%	ISOETHARINE HYDROCHLORIDE		Discontinued	No
017796	NDA	SANOFI AVENTIS US	001	BRYREL	SYRUP;ORAL	EQ 500MG BASE/5ML	PIPERAZINE CITRATE		Discontinued	No
017497	NDA	SANOFI AVENTIS US	001	CALCIMAR	INJECTABLE;INJECTION	400 IU/VIAL	CALCITONIN SALMON		Discontinued	No
018237	NDA	SANOFI AVENTIS US	001	CALCIPARINE	INJECTABLE;INJECTION	25,000 UNITS/ML	HEPARIN CALCIUM		Discontinued	No
080564	ANDA	SANOFI AVENTIS US	001	CYANOCOBALAMIN	INJECTABLE;INJECTION	1MG/ML	CYANOCOBALAMIN		Discontinued	No
083517	ANDA	SANOFI AVENTIS US	001	DV	SUPPOSITORY;VAGINAL	0.7MG	DIENESTROL		Discontinued	No
083518	ANDA	SANOFI AVENTIS US	001	DV	CREAM;VAGINAL	0.01%	DIENESTROL		Discontinued	No
008767	NDA	SANOFI AVENTIS US	002	HEDULIN	TABLET;ORAL	50MG	PHENINDIONE		Discontinued	No
016990	NDA	SANOFI AVENTIS US	001	INTAL	CAPSULE;INHALATION	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CROMOLYN SODIUM		Discontinued	No
006327	NDA	SANOFI AVENTIS US	002	ISUPREL	SOLUTION;INHALATION	0.5%	ISOPROTERENOL HYDROCHLORIDE		Discontinued	No
006327	NDA	SANOFI AVENTIS US	003	ISUPREL	SOLUTION;INHALATION	1%	ISOPROTERENOL HYDROCHLORIDE		Discontinued	No
011178	NDA	SANOFI AVENTIS US	001	ISUPREL	AEROSOL, METERED;INHALATION	0.103MG/INH	ISOPROTERENOL HYDROCHLORIDE		Discontinued	No
012594	NDA	SANOFI AVENTIS US	001	METAHYDRIN	TABLET;ORAL	2MG	TRICHLORMETHIAZIDE		Discontinued	No
012594	NDA	SANOFI AVENTIS US	002	METAHYDRIN	TABLET;ORAL	4MG	TRICHLORMETHIAZIDE		Discontinued	No
012972	NDA	SANOFI AVENTIS US	001	METATENSIN #2	TABLET;ORAL	0.1MG;2MG	RESERPINE; TRICHLORMETHIAZIDE		Discontinued	No
012972	NDA	SANOFI AVENTIS US	002	METATENSIN #4	TABLET;ORAL	0.1MG;4MG	RESERPINE; TRICHLORMETHIAZIDE		Discontinued	No
019498	NDA	SANOFI AVENTIS US	001	PARATHAR	INJECTABLE;INJECTION	200 UNITS/VIAL	TERIPARATIDE ACETATE		Discontinued	No
008402	NDA	SANOFI AVENTIS US	001	PHISOHEX	EMULSION;TOPICAL	3%	HEXACHLOROPHENE		Discontinued	No
085203	ANDA	SANOFI AVENTIS US	001	SLO-PHYLLIN	CAPSULE, EXTENDED RELEASE;ORAL	125MG	THEOPHYLLINE		Discontinued	No
085205	ANDA	SANOFI AVENTIS US	001	SLO-PHYLLIN	CAPSULE, EXTENDED RELEASE;ORAL	250MG	THEOPHYLLINE		Discontinued	No
085206	ANDA	SANOFI AVENTIS US	001	SLO-PHYLLIN	CAPSULE, EXTENDED RELEASE;ORAL	60MG	THEOPHYLLINE		Discontinued	No
008102	NDA	SANOFI AVENTIS US	004	TACE	CAPSULE;ORAL	12MG	CHLOROTRIANISENE		Discontinued	No
011444	NDA	SANOFI AVENTIS US	001	TACE	CAPSULE;ORAL	25MG	CHLOROTRIANISENE		Discontinued	No
016235	NDA	SANOFI AVENTIS US	001	TACE	CAPSULE;ORAL	72MG	CHLOROTRIANISENE		Discontinued	No
016809	NDA	SANOFI AVENTIS US	002	TRICLOS	TABLET;ORAL	750MG	TRICLOFOS SODIUM		Discontinued	No
016830	NDA	SANOFI AVENTIS US	001	TRICLOS	SOLUTION;ORAL	1.5GM/15ML	TRICLOFOS SODIUM		Discontinued	No
061596	ANDA	SANOFI AVENTIS US	001	VANOBID	OINTMENT;VAGINAL	0.6MG/GM	CANDICIDIN		Discontinued	No
061613	ANDA	SANOFI AVENTIS US	001	VANOBID	TABLET;VAGINAL	3MG	CANDICIDIN		Discontinued	No
083459	ANDA	SANOFI AVENTIS US	001	VENTAIRE	TABLET;ORAL	2MG	PROTOKYLOL HYDROCHLORIDE		Discontinued	No
016732	NDA	SANOFI AVENTIS US	001	TALWIN 50	TABLET;ORAL	EQ 50MG BASE	PENTAZOCINE HYDROCHLORIDE	1969-02-03	Discontinued	No
014860	NDA	SANOFI AVENTIS US	002	ARALEN PHOSPHATE W/ PRIMAQUINE PHOSPHATE	TABLET;ORAL	EQ 300MG BASE;EQ 45MG BASE	CHLOROQUINE PHOSPHATE; PRIMAQUINE PHOSPHATE	1968-12-09	Discontinued	No
013621	NDA	SANOFI AVENTIS US	001	PERTOFRANE	CAPSULE;ORAL	25MG	DESIPRAMINE HYDROCHLORIDE	1968-04-10	Discontinued	No
013621	NDA	SANOFI AVENTIS US	002	PERTOFRANE	CAPSULE;ORAL	50MG	DESIPRAMINE HYDROCHLORIDE	1968-04-10	Discontinued	No
016363	NDA	SANOFI AVENTIS US	001	LASIX	INJECTABLE;INJECTION	10MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	FUROSEMIDE	1968-03-20	Discontinued	No
016131	NDA	SANOFI AVENTIS US	002	CLOMID	TABLET;ORAL	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CLOMIPHENE CITRATE	1967-02-01	Discontinued	No
015103	NDA	SANOFI AVENTIS US	002	DEMI-REGROTON	TABLET;ORAL	25MG;0.125MG	CHLORTHALIDONE; RESERPINE	1964-05-08	Discontinued	No
015103	NDA	SANOFI AVENTIS US	001	REGROTON	TABLET;ORAL	50MG;0.25MG	CHLORTHALIDONE; RESERPINE	1964-05-08	Discontinued	No
014214	NDA	SANOFI AVENTIS US	002	NEGGRAM	TABLET;ORAL	250MG	NALIDIXIC ACID	1964-03-06	Discontinued	No
			004	NEGGRAM	TABLET;ORAL	500MG	NALIDIXIC ACID	1964-03-06	Discontinued	No
			005	NEGGRAM	TABLET;ORAL	1GM	NALIDIXIC ACID	1964-03-06	Discontinued	No
011467	NDA	SANOFI AVENTIS US	003	TRANCOPAL	TABLET;ORAL	100MG	CHLORMEZANONE	1960-05-20	Discontinued	No
011467	NDA	SANOFI AVENTIS US	005	TRANCOPAL	TABLET;ORAL	200MG	CHLORMEZANONE	1960-05-20	Discontinued	No
012283	NDA	SANOFI AVENTIS US	003	HYGROTON	TABLET;ORAL	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CHLORTHALIDONE	1960-04-07	Discontinued	No
012283	NDA	SANOFI AVENTIS US	004	HYGROTON	TABLET;ORAL	25MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CHLORTHALIDONE	1960-04-07	Discontinued	No
011836	NDA	SANOFI AVENTIS US	003	PRESAMINE	TABLET;ORAL	25MG	IMIPRAMINE HYDROCHLORIDE	1959-04-16	Discontinued	No
			006	PRESAMINE	TABLET;ORAL	10MG	IMIPRAMINE HYDROCHLORIDE	1959-04-16	Discontinued	No
			007	PRESAMINE	TABLET;ORAL	50MG	IMIPRAMINE HYDROCHLORIDE	1959-04-16	Discontinued	No
010787	NDA	SANOFI AVENTIS US	002	IRON DEXTRAN	INJECTABLE;INJECTION	EQ 50MG IRON/ML	IRON DEXTRAN	1957-04-25	Discontinued	No
009519	NDA	SANOFI AVENTIS US	002	DORIDEN	TABLET;ORAL	250MG	GLUTETHIMIDE	1957-04-16	Discontinued	No
			005	DORIDEN	TABLET;ORAL	500MG	GLUTETHIMIDE	1957-04-16	Discontinued	No
			008	DORIDEN	CAPSULE;ORAL	500MG	GLUTETHIMIDE	1957-04-16	Discontinued	No
010679	NDA	SANOFI AVENTIS US	003	CANTIL	TABLET;ORAL	25MG	MEPENZOLATE BROMIDE	1956-11-14	Discontinued	No
010679	NDA	SANOFI AVENTIS US	004	CANTIL	SOLUTION;ORAL	25MG/5ML	MEPENZOLATE BROMIDE	1956-11-14	Discontinued	No
010598	NDA	SANOFI AVENTIS US	002	BENDECTIN	TABLET, EXTENDED RELEASE;ORAL	10MG;10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE	1956-07-30	Discontinued	No
010155	NDA	SANOFI AVENTIS US	002	MYTELASE	TABLET;ORAL	10MG	AMBENONIUM CHLORIDE	1956-05-01	Discontinued	No
009410	NDA	SANOFI AVENTIS US	005	LOTUSATE	TABLET;ORAL	120MG	TALBUTAL	1954-09-21	Discontinued	No
009166	NDA	SANOFI AVENTIS US	001	HYDROXYSTILBAMIDINE ISETHIONATE	INJECTABLE;INJECTION	225MG/AMP	HYDROXYSTILBAMIDINE ISETHIONATE	1953-12-22	Discontinued	No
008316	NDA	SANOFI AVENTIS US	001	PRIMAQUINE	TABLET;ORAL	EQ 15MG BASE	PRIMAQUINE PHOSPHATE	1952-01-23	Prescription	Yes
007504	NDA	SANOFI AVENTIS US	002	ACTHAR	INJECTABLE;INJECTION	25 UNITS/VIAL	CORTICOTROPIN	1950-07-03	Discontinued	No
007504	NDA	SANOFI AVENTIS US	003	ACTHAR	INJECTABLE;INJECTION	40 UNITS/VIAL	CORTICOTROPIN	1950-07-03	Discontinued	No
006002	NDA	SANOFI AVENTIS US	001	ARALEN	TABLET;ORAL	500MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CHLOROQUINE PHOSPHATE	1949-10-31	Discontinued	No
006002	NDA	SANOFI AVENTIS US	002	ARALEN HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 40MG BASE/ML	CHLOROQUINE HYDROCHLORIDE	1949-10-31	Discontinued	No
006882	NDA	SANOFI AVENTIS US	001	PHISOHEX	EMULSION;TOPICAL	3%	HEXACHLOROPHENE	1949-04-19	Discontinued	No
006412	NDA	SANOFI AVENTIS US	014	DECAPRYN	TABLET;ORAL	25MG	DOXYLAMINE SUCCINATE	1948-04-07	Discontinued	No
006412	NDA	SANOFI AVENTIS US	015	DECAPRYN	TABLET;ORAL	12.5MG	DOXYLAMINE SUCCINATE	1948-04-07	Discontinued	No
006328	NDA	SANOFI AVENTIS US	001	ISUPREL	TABLET;RECTAL, SUBLINGUAL	10MG	ISOPROTERENOL HYDROCHLORIDE	1948-02-19	Discontinued	No
006328	NDA	SANOFI AVENTIS US	002	ISUPREL	TABLET;RECTAL, SUBLINGUAL	15MG	ISOPROTERENOL HYDROCHLORIDE	1948-02-19	Discontinued	No