RANBAXY LABORATORIES LIMITED Discontinued
FDA Approved Drugs
RANBAXY LABORATORIES LIMITED Discontinued
FDA Approved Drugs Database
FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.
- Total Records 88
- Latest Approval Date Mar 06, 2009
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Overview
Company
RANBAXY LABORATORIES LIMITED Discontinued
Country
India
Website
Social Profiles
Company Snapshot
RANBAXY LABORATORIES LIMITED Discontinued
Plot 90, Sector 32,Gurgaon-122001 (Haryana)
India
ranbaxy.com corporate.communications@ranbaxy.com View on MapFDA Approved Drug Records ( 88 records )
Drug Name
ACYCLOVIR
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1998-09-30
Active Ingredient
ACYCLOVIR
Application Number
74975
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1998-09-30
Regulatory Status
Discontinued
Drug Name
AVENTYL
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
NORTRIPTYLINE HYDROCHLORIDE
Application Number
14685
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CARBILEV
Product Number
1
Dosage Form
-
Strength
10MG;100MG
Approval Date
2005-06-10
Active Ingredient
CARBIDOPA; LEVODOPA
Application Number
76643
Product Number
1
Dosage Form
-
Strength
10MG;100MG
Approval Date
2005-06-10
Regulatory Status
Discontinued
Drug Name
CARBILEV
Product Number
2
Dosage Form
-
Strength
25MG;100MG
Approval Date
2005-06-10
Active Ingredient
CARBIDOPA; LEVODOPA
Application Number
76643
Product Number
2
Dosage Form
-
Strength
25MG;100MG
Approval Date
2005-06-10
Regulatory Status
Discontinued
Drug Name
CARBILEV
Product Number
3
Dosage Form
-
Strength
25MG;250MG
Approval Date
2005-06-10
Active Ingredient
CARBIDOPA; LEVODOPA
Application Number
76643
Product Number
3
Dosage Form
-
Strength
25MG;250MG
Approval Date
2005-06-10
Regulatory Status
Discontinued
Drug Name
CEFACLOR
Product Number
1
Dosage Form
-
Strength
EQ 375MG BASE/5ML
Approval Date
1997-10-02
Active Ingredient
CEFACLOR
Application Number
64155
Product Number
1
Dosage Form
-
Strength
EQ 375MG BASE/5ML
Approval Date
1997-10-02
Regulatory Status
Discontinued
Drug Name
CEFACLOR
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1997-08-28
Active Ingredient
CEFACLOR
Application Number
64156
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1997-08-28
Regulatory Status
Discontinued
Drug Name
CEFACLOR
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1997-08-28
Active Ingredient
CEFACLOR
Application Number
64156
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1997-08-28
Regulatory Status
Discontinued
Drug Name
CEFACLOR
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/5ML
Approval Date
1997-10-02
Active Ingredient
CEFACLOR
Application Number
64164
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/5ML
Approval Date
1997-10-02
Regulatory Status
Discontinued
Drug Name
CEFACLOR
Product Number
1
Dosage Form
-
Strength
EQ 187MG BASE/5ML
Approval Date
1997-10-02
Active Ingredient
CEFACLOR
Application Number
64165
Product Number
1
Dosage Form
-
Strength
EQ 187MG BASE/5ML
Approval Date
1997-10-02
Regulatory Status
Discontinued
Drug Name
CEFACLOR
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE/5ML
Approval Date
1997-10-02
Active Ingredient
CEFACLOR
Application Number
64166
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE/5ML
Approval Date
1997-10-02
Regulatory Status
Discontinued
Drug Name
CEFADROXIL
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1999-06-22
Active Ingredient
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Application Number
65015
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1999-06-22
Regulatory Status
Discontinued
Drug Name
CEFADROXIL
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE
Approval Date
1999-04-23
Active Ingredient
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Application Number
65018
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE
Approval Date
1999-04-23
Regulatory Status
Discontinued
Drug Name
CEFPROZIL
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
2006-12-13
Active Ingredient
CEFPROZIL
Application Number
65198
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
2006-12-13
Regulatory Status
Discontinued
Drug Name
CEFPROZIL
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
2006-12-13
Active Ingredient
CEFPROZIL
Application Number
65198
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
2006-12-13
Regulatory Status
Discontinued
Drug Name
CEFPROZIL
Product Number
1
Dosage Form
-
Strength
125MG/5ML
Approval Date
2006-06-30
Active Ingredient
CEFPROZIL
Application Number
65202
Product Number
1
Dosage Form
-
Strength
125MG/5ML
Approval Date
2006-06-30
Regulatory Status
Discontinued
Drug Name
CEFPROZIL
Product Number
2
Dosage Form
-
Strength
250MG/5ML
Approval Date
2006-06-30
Active Ingredient
CEFPROZIL
Application Number
65202
Product Number
2
Dosage Form
-
Strength
250MG/5ML
Approval Date
2006-06-30
Regulatory Status
Discontinued
Drug Name
CEFUROXIME AXETIL
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
2002-02-15
Active Ingredient
CEFUROXIME AXETIL
Application Number
65043
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
2002-02-15
Regulatory Status
Discontinued
Drug Name
CEFUROXIME AXETIL
Product Number
2
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
2002-02-15
Active Ingredient
CEFUROXIME AXETIL
Application Number
65043
Product Number
2
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
2002-02-15
Regulatory Status
Discontinued
Drug Name
CEFUROXIME AXETIL
Product Number
3
Dosage Form
-
Strength
EQ 125MG BASE
Approval Date
2002-02-15
Active Ingredient
CEFUROXIME AXETIL
Application Number
65043
Product Number
3
Dosage Form
-
Strength
EQ 125MG BASE
Approval Date
2002-02-15
Regulatory Status
Discontinued
Drug Name
CETIRIZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
5MG/5ML
Approval Date
2008-06-18
Active Ingredient
CETIRIZINE HYDROCHLORIDE
Application Number
77472
Product Number
1
Dosage Form
-
Strength
5MG/5ML
Approval Date
2008-06-18
Regulatory Status
Discontinued
Drug Name
CHILDRENS CETIRIZINE HYDROCHLORIDE ALLERGY
Product Number
2
Dosage Form
-
Strength
5MG/5ML
Approval Date
2008-04-24
Active Ingredient
CETIRIZINE HYDROCHLORIDE
Application Number
90183
Product Number
2
Dosage Form
-
Strength
5MG/5ML
Approval Date
2008-04-24
Regulatory Status
Discontinued
Drug Name
CHILDRENS CETIRIZINE HYDROCHLORIDE HIVES RELIEF
Product Number
1
Dosage Form
-
Strength
5MG/5ML
Approval Date
2008-04-24
Active Ingredient
CETIRIZINE HYDROCHLORIDE
Application Number
90183
Product Number
1
Dosage Form
-
Strength
5MG/5ML
Approval Date
2008-04-24
Regulatory Status
Discontinued
Drug Name
CHLORZOXAZONE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1993-12-29
Active Ingredient
CHLORZOXAZONE
Application Number
81298
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1993-12-29
Regulatory Status
Discontinued
Drug Name
CHLORZOXAZONE
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1993-12-29
Active Ingredient
CHLORZOXAZONE
Application Number
81299
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1993-12-29
Regulatory Status
Discontinued
Drug Name
CLARITHROMYCIN
Product Number
1
Dosage Form
-
Strength
1GM
Approval Date
2005-01-26
Active Ingredient
CLARITHROMYCIN
Application Number
65210
Product Number
1
Dosage Form
-
Strength
1GM
Approval Date
2005-01-26
Regulatory Status
Discontinued
Drug Name
DISPERMOX
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
2003-08-11
Active Ingredient
AMOXICILLIN
Application Number
65080
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
2003-08-11
Regulatory Status
Discontinued
Drug Name
DISPERMOX
Product Number
2
Dosage Form
-
Strength
200MG
Approval Date
2003-08-11
Active Ingredient
AMOXICILLIN
Application Number
65080
Product Number
2
Dosage Form
-
Strength
200MG
Approval Date
2003-08-11
Regulatory Status
Discontinued
Drug Name
DISPERMOX
Product Number
1
Dosage Form
-
Strength
600MG
Approval Date
2003-12-04
Active Ingredient
AMOXICILLIN
Application Number
65159
Product Number
1
Dosage Form
-
Strength
600MG
Approval Date
2003-12-04
Regulatory Status
Discontinued
Drug Name
DOXYCYCLINE HYCLATE
Product Number
1
Dosage Form
-
Strength
EQ 50MG BASE
Approval Date
1983-12-23
Active Ingredient
DOXYCYCLINE HYCLATE
Application Number
62479
Product Number
1
Dosage Form
-
Strength
EQ 50MG BASE
Approval Date
1983-12-23
Regulatory Status
Discontinued
Drug Name
DOXYCYCLINE HYCLATE
Product Number
2
Dosage Form
-
Strength
EQ 100MG BASE
Approval Date
1983-12-23
Active Ingredient
DOXYCYCLINE HYCLATE
Application Number
62479
Product Number
2
Dosage Form
-
Strength
EQ 100MG BASE
Approval Date
1983-12-23
Regulatory Status
Discontinued
Drug Name
ETODOLAC
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
1998-11-24
Active Ingredient
ETODOLAC
Application Number
75226
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
1998-11-24
Regulatory Status
Discontinued
Drug Name
ETODOLAC
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1998-11-24
Active Ingredient
ETODOLAC
Application Number
75226
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1998-11-24
Regulatory Status
Discontinued
Drug Name
FLUCONAZOLE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
2004-07-29
Active Ingredient
FLUCONAZOLE
Application Number
76386
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
2004-07-29
Regulatory Status
Discontinued
Drug Name
FLUCONAZOLE
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
2004-07-29
Active Ingredient
FLUCONAZOLE
Application Number
76386
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
2004-07-29
Regulatory Status
Discontinued
Drug Name
FLUCONAZOLE
Product Number
3
Dosage Form
-
Strength
150MG
Approval Date
2004-07-29
Active Ingredient
FLUCONAZOLE
Application Number
76386
Product Number
3
Dosage Form
-
Strength
150MG
Approval Date
2004-07-29
Regulatory Status
Discontinued
Drug Name
FLUCONAZOLE
Product Number
4
Dosage Form
-
Strength
200MG
Approval Date
2004-07-29
Active Ingredient
FLUCONAZOLE
Application Number
76386
Product Number
4
Dosage Form
-
Strength
200MG
Approval Date
2004-07-29
Regulatory Status
Discontinued
Drug Name
FOSINOPRIL SODIUM
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
2004-04-23
Active Ingredient
FOSINOPRIL SODIUM
Application Number
76580
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
2004-04-23
Regulatory Status
Discontinued
Drug Name
FOSINOPRIL SODIUM
Product Number
2
Dosage Form
-
Strength
20MG
Approval Date
2004-04-23
Active Ingredient
FOSINOPRIL SODIUM
Application Number
76580
Product Number
2
Dosage Form
-
Strength
20MG
Approval Date
2004-04-23
Regulatory Status
Discontinued
Drug Name
FOSINOPRIL SODIUM
Product Number
3
Dosage Form
-
Strength
40MG
Approval Date
2004-04-23
Active Ingredient
FOSINOPRIL SODIUM
Application Number
76580
Product Number
3
Dosage Form
-
Strength
40MG
Approval Date
2004-04-23
Regulatory Status
Discontinued
Drug Name
GABAPENTIN
Product Number
1
Dosage Form
-
Strength
600MG
Approval Date
2005-09-14
Active Ingredient
GABAPENTIN
Application Number
76605
Product Number
1
Dosage Form
-
Strength
600MG
Approval Date
2005-09-14
Regulatory Status
Discontinued
Drug Name
GABAPENTIN
Product Number
2
Dosage Form
-
Strength
800MG
Approval Date
2005-09-14
Active Ingredient
GABAPENTIN
Application Number
76605
Product Number
2
Dosage Form
-
Strength
800MG
Approval Date
2005-09-14
Regulatory Status
Discontinued
Drug Name
GANCICLOVIR
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
2003-06-27
Active Ingredient
GANCICLOVIR
Application Number
76457
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
2003-06-27
Regulatory Status
Discontinued
Drug Name
GANCICLOVIR
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
2003-06-27
Active Ingredient
GANCICLOVIR
Application Number
76457
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
2003-06-27
Regulatory Status
Discontinued
Drug Name
GLIMEPIRIDE
Product Number
1
Dosage Form
-
Strength
1MG
Approval Date
2005-10-06
Active Ingredient
GLIMEPIRIDE
Application Number
76875
Product Number
1
Dosage Form
-
Strength
1MG
Approval Date
2005-10-06
Regulatory Status
Discontinued
Drug Name
GLIMEPIRIDE
Product Number
2
Dosage Form
-
Strength
2MG
Approval Date
2005-10-06
Active Ingredient
GLIMEPIRIDE
Application Number
76875
Product Number
2
Dosage Form
-
Strength
2MG
Approval Date
2005-10-06
Regulatory Status
Discontinued
Drug Name
GLIMEPIRIDE
Product Number
3
Dosage Form
-
Strength
4MG
Approval Date
2005-10-06
Active Ingredient
GLIMEPIRIDE
Application Number
76875
Product Number
3
Dosage Form
-
Strength
4MG
Approval Date
2005-10-06
Regulatory Status
Discontinued
Drug Name
GLIMEPIRIDE
Product Number
4
Dosage Form
-
Strength
8MG
Approval Date
2005-10-06
Active Ingredient
GLIMEPIRIDE
Application Number
76875
Product Number
4
Dosage Form
-
Strength
8MG
Approval Date
2005-10-06
Regulatory Status
Discontinued
Drug Name
GLIMEPIRIDE
Product Number
1
Dosage Form
-
Strength
3MG
Approval Date
2005-10-06
Active Ingredient
GLIMEPIRIDE
Application Number
77366
Product Number
1
Dosage Form
-
Strength
3MG
Approval Date
2005-10-06
Regulatory Status
Discontinued
Drug Name
GLIMEPIRIDE
Product Number
2
Dosage Form
-
Strength
6MG
Approval Date
2005-10-06
Active Ingredient
GLIMEPIRIDE
Application Number
77366
Product Number
2
Dosage Form
-
Strength
6MG
Approval Date
2005-10-06
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
2007-08-16
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
40822
Product Number
1
Dosage Form
-
Strength
750MG;7.5MG
Approval Date
2007-08-16
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;10MG
Approval Date
2007-08-16
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
40824
Product Number
1
Dosage Form
-
Strength
500MG;10MG
Approval Date
2007-08-16
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
2007-08-16
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
40825
Product Number
1
Dosage Form
-
Strength
500MG;5MG
Approval Date
2007-08-16
Regulatory Status
Discontinued
Drug Name
IBUPROFEN
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
1985-12-26
Active Ingredient
IBUPROFEN
Application Number
70818
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
1985-12-26
Regulatory Status
Discontinued
Drug Name
IBUPROFEN
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1986-07-15
Active Ingredient
IBUPROFEN
Application Number
71163
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1986-07-15
Regulatory Status
Discontinued
Drug Name
IBUPROHM
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
1985-08-29
Active Ingredient
IBUPROFEN
Application Number
70469
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
1985-08-29
Regulatory Status
Discontinued
Drug Name
IBUPROHM
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1986-12-01
Active Ingredient
IBUPROFEN
Application Number
71214
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1986-12-01
Regulatory Status
Discontinued
Drug Name
IBUPROHM COLD AND SINUS
Product Number
1
Dosage Form
-
Strength
200MG;30MG
Approval Date
2001-04-17
Active Ingredient
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
Application Number
74567
Product Number
1
Dosage Form
-
Strength
200MG;30MG
Approval Date
2001-04-17
Regulatory Status
Discontinued
Drug Name
LORATADINE
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
2004-08-20
Active Ingredient
LORATADINE
Application Number
76529
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
2004-08-20
Regulatory Status
Discontinued
Drug Name
METFORMIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
2004-06-18
Active Ingredient
METFORMIN HYDROCHLORIDE
Application Number
76413
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
2004-06-18
Regulatory Status
Discontinued
Drug Name
METFORMIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
750MG
Approval Date
2005-06-29
Active Ingredient
METFORMIN HYDROCHLORIDE
Application Number
77211
Product Number
1
Dosage Form
-
Strength
750MG
Approval Date
2005-06-29
Regulatory Status
Discontinued
Drug Name
NITROFURANTOIN (MONOHYDRATE/MACROCRYSTALS)
Product Number
1
Dosage Form
-
Strength
75MG;25MG
Approval Date
2005-03-30
Active Ingredient
NITROFURANTOIN; NITROFURANTOIN, MACROCRYSTALLINE
Application Number
76951
Product Number
1
Dosage Form
-
Strength
75MG;25MG
Approval Date
2005-03-30
Regulatory Status
Discontinued
Drug Name
OFLOXACIN
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
2003-09-02
Active Ingredient
OFLOXACIN
Application Number
76220
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
2003-09-02
Regulatory Status
Discontinued
Drug Name
OFLOXACIN
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
2003-09-02
Active Ingredient
OFLOXACIN
Application Number
76220
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
2003-09-02
Regulatory Status
Discontinued
Drug Name
OFLOXACIN
Product Number
3
Dosage Form
-
Strength
400MG
Approval Date
2003-09-02
Active Ingredient
OFLOXACIN
Application Number
76220
Product Number
3
Dosage Form
-
Strength
400MG
Approval Date
2003-09-02
Regulatory Status
Discontinued
Drug Name
PANIXINE DISPERDOSE
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
2003-09-11
Active Ingredient
CEPHALEXIN
Application Number
65100
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
2003-09-11
Regulatory Status
Discontinued
Drug Name
PANIXINE DISPERDOSE
Product Number
2
Dosage Form
-
Strength
EQ 125MG BASE
Approval Date
2003-09-11
Active Ingredient
CEPHALEXIN
Application Number
65100
Product Number
2
Dosage Form
-
Strength
EQ 125MG BASE
Approval Date
2003-09-11
Regulatory Status
Discontinued
Drug Name
PRAVASTATIN SODIUM
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
2007-04-23
Active Ingredient
PRAVASTATIN SODIUM
Application Number
76445
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
2007-04-23
Regulatory Status
Discontinued
Drug Name
PRAVASTATIN SODIUM
Product Number
2
Dosage Form
-
Strength
20MG
Approval Date
2007-04-23
Active Ingredient
PRAVASTATIN SODIUM
Application Number
76445
Product Number
2
Dosage Form
-
Strength
20MG
Approval Date
2007-04-23
Regulatory Status
Discontinued
Drug Name
PRAVASTATIN SODIUM
Product Number
3
Dosage Form
-
Strength
40MG
Approval Date
2007-04-23
Active Ingredient
PRAVASTATIN SODIUM
Application Number
76445
Product Number
3
Dosage Form
-
Strength
40MG
Approval Date
2007-04-23
Regulatory Status
Discontinued
Drug Name
PRAVASTATIN SODIUM
Product Number
4
Dosage Form
-
Strength
80MG
Approval Date
2007-04-23
Active Ingredient
PRAVASTATIN SODIUM
Application Number
76445
Product Number
4
Dosage Form
-
Strength
80MG
Approval Date
2007-04-23
Regulatory Status
Discontinued
Drug Name
RAMIPRIL
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2009-03-06
Active Ingredient
RAMIPRIL
Application Number
78849
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2009-03-06
Regulatory Status
Discontinued
Drug Name
RAMIPRIL
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
2009-03-06
Active Ingredient
RAMIPRIL
Application Number
78849
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
2009-03-06
Regulatory Status
Discontinued
Drug Name
RANICLOR
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE
Approval Date
2003-12-22
Active Ingredient
CEFACLOR
Application Number
65092
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE
Approval Date
2003-12-22
Regulatory Status
Discontinued
Drug Name
RANICLOR
Product Number
2
Dosage Form
-
Strength
EQ 187MG BASE
Approval Date
2003-12-22
Active Ingredient
CEFACLOR
Application Number
65092
Product Number
2
Dosage Form
-
Strength
EQ 187MG BASE
Approval Date
2003-12-22
Regulatory Status
Discontinued
Drug Name
RANICLOR
Product Number
3
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
2003-12-22
Active Ingredient
CEFACLOR
Application Number
65092
Product Number
3
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
2003-12-22
Regulatory Status
Discontinued
Drug Name
RANICLOR
Product Number
4
Dosage Form
-
Strength
EQ 375MG BASE
Approval Date
2003-12-22
Active Ingredient
CEFACLOR
Application Number
65092
Product Number
4
Dosage Form
-
Strength
EQ 375MG BASE
Approval Date
2003-12-22
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE
Approval Date
1998-01-30
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
75000
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE
Approval Date
1998-01-30
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 300MG BASE
Approval Date
1998-01-30
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
75000
Product Number
2
Dosage Form
-
Strength
EQ 300MG BASE
Approval Date
1998-01-30
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
2000-01-14
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
75254
Product Number
1
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
2000-01-14
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 15MG BASE/ML
Approval Date
2007-12-13
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
78448
Product Number
1
Dosage Form
-
Strength
EQ 15MG BASE/ML
Approval Date
2007-12-13
Regulatory Status
Discontinued
Drug Name
RIOMET
Product Number
1
Dosage Form
-
Strength
500MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-09-11
Active Ingredient
METFORMIN HYDROCHLORIDE
Application Number
21591
Product Number
1
Dosage Form
-
Strength
500MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-09-11
Regulatory Status
Discontinued
Drug Name
SERTRALINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
2007-02-05
Active Ingredient
SERTRALINE HYDROCHLORIDE
Application Number
78053
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
2007-02-05
Regulatory Status
Discontinued
Drug Name
TERAZOSIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE
Approval Date
2002-08-22
Active Ingredient
TERAZOSIN HYDROCHLORIDE
Application Number
76021
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE
Approval Date
2002-08-22
Regulatory Status
Discontinued
Drug Name
TERAZOSIN HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2002-08-22
Active Ingredient
TERAZOSIN HYDROCHLORIDE
Application Number
76021
Product Number
2
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2002-08-22
Regulatory Status
Discontinued
Drug Name
TERAZOSIN HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
EQ 5MG BASE
Approval Date
2002-08-22
Active Ingredient
TERAZOSIN HYDROCHLORIDE
Application Number
76021
Product Number
3
Dosage Form
-
Strength
EQ 5MG BASE
Approval Date
2002-08-22
Regulatory Status
Discontinued
Drug Name
TERAZOSIN HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
EQ 10MG BASE
Approval Date
2002-08-22
Active Ingredient
TERAZOSIN HYDROCHLORIDE
Application Number
76021
Product Number
4
Dosage Form
-
Strength
EQ 10MG BASE
Approval Date
2002-08-22
Regulatory Status
Discontinued
Drug Name
ZIDOVUDINE
Product Number
1
Dosage Form
-
Strength
300MG
Approval Date
2005-09-19
Active Ingredient
ZIDOVUDINE
Application Number
77327
Product Number
1
Dosage Form
-
Strength
300MG
Approval Date
2005-09-19
Regulatory Status
Discontinued
Drug Status Breakdown
88 total- Discontinued
Official Source
FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.
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Drug Name
ACYCLOVIR
Application Number
74975
Product Number
1
Active Ingredient
ACYCLOVIR
Dosage Form
-
Strength
200MG
FDA Approved Drug Data
Approved drug product information
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