Boehringer Ingelheim GmbH Discontinued
FDA Approved Drugs
Boehringer Ingelheim GmbH 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 59
- Latest Approval Date Nov 08, 2012
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Overview
Company
Boehringer Ingelheim GmbH Discontinued
Country
Germany
Website
Social Profiles
Company Snapshot
Boehringer Ingelheim GmbH Discontinued
Corporate Division Communications, Binger Strasse 173, 55216 Ingelheim am Rhein
Germany
www.boehringer-ingelheim.com/ info@boehringer-ingelheim.de View on MapFDA Approved Drug Records ( 59 records )
Drug Name
AGGRENOX
Product Number
1
Dosage Form
-
Strength
25MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1999-11-22
Active Ingredient
ASPIRIN; DIPYRIDAMOLE
Application Number
20884
Product Number
1
Dosage Form
-
Strength
25MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1999-11-22
Regulatory Status
Discontinued
Drug Name
ALUPENT
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1982-01-01
Active Ingredient
METAPROTERENOL SULFATE
Application Number
15874
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALUPENT
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Active Ingredient
METAPROTERENOL SULFATE
Application Number
15874
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALUPENT
Product Number
1
Dosage Form
-
Strength
0.65MG/INH
Approval Date
1982-01-01
Active Ingredient
METAPROTERENOL SULFATE
Application Number
16402
Product Number
1
Dosage Form
-
Strength
0.65MG/INH
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALUPENT
Product Number
1
Dosage Form
-
Strength
10MG/5ML
Approval Date
1982-01-01
Active Ingredient
METAPROTERENOL SULFATE
Application Number
17571
Product Number
1
Dosage Form
-
Strength
10MG/5ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALUPENT
Product Number
1
Dosage Form
-
Strength
5%
Approval Date
1982-01-01
Active Ingredient
METAPROTERENOL SULFATE
Application Number
17659
Product Number
1
Dosage Form
-
Strength
5%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ALUPENT
Product Number
1
Dosage Form
-
Strength
0.6%
Approval Date
1983-06-30
Active Ingredient
METAPROTERENOL SULFATE
Application Number
18761
Product Number
1
Dosage Form
-
Strength
0.6%
Approval Date
1983-06-30
Regulatory Status
Discontinued
Drug Name
ALUPENT
Product Number
2
Dosage Form
-
Strength
0.4%
Approval Date
1986-10-10
Active Ingredient
METAPROTERENOL SULFATE
Application Number
18761
Product Number
2
Dosage Form
-
Strength
0.4%
Approval Date
1986-10-10
Regulatory Status
Discontinued
Drug Name
APTIVUS
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
2008-06-23
Active Ingredient
TIPRANAVIR
Application Number
22292
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
2008-06-23
Regulatory Status
Discontinued
Drug Name
ATROVENT
Product Number
1
Dosage Form
-
Strength
0.018MG/INH
Approval Date
1986-12-29
Active Ingredient
IPRATROPIUM BROMIDE
Application Number
19085
Product Number
1
Dosage Form
-
Strength
0.018MG/INH
Approval Date
1986-12-29
Regulatory Status
Discontinued
Drug Name
ATROVENT
Product Number
1
Dosage Form
-
Strength
0.02% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-09-29
Active Ingredient
IPRATROPIUM BROMIDE
Application Number
20228
Product Number
1
Dosage Form
-
Strength
0.02% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-09-29
Regulatory Status
Discontinued
Drug Name
ATROVENT
Product Number
1
Dosage Form
-
Strength
0.021MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-10-20
Active Ingredient
IPRATROPIUM BROMIDE
Application Number
20393
Product Number
1
Dosage Form
-
Strength
0.021MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-10-20
Regulatory Status
Discontinued
Drug Name
ATROVENT
Product Number
1
Dosage Form
-
Strength
0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-10-20
Active Ingredient
IPRATROPIUM BROMIDE
Application Number
20394
Product Number
1
Dosage Form
-
Strength
0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-10-20
Regulatory Status
Discontinued
Drug Name
CATAPRES
Product Number
1
Dosage Form
-
Strength
0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CLONIDINE HYDROCHLORIDE
Application Number
17407
Product Number
1
Dosage Form
-
Strength
0.1MG **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
CATAPRES
Product Number
2
Dosage Form
-
Strength
0.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CLONIDINE HYDROCHLORIDE
Application Number
17407
Product Number
2
Dosage Form
-
Strength
0.2MG **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
CATAPRES
Product Number
3
Dosage Form
-
Strength
0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CLONIDINE HYDROCHLORIDE
Application Number
17407
Product Number
3
Dosage Form
-
Strength
0.3MG **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
COMBIPRES
Product Number
1
Dosage Form
-
Strength
15MG;0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE
Application Number
17503
Product Number
1
Dosage Form
-
Strength
15MG;0.1MG **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
COMBIPRES
Product Number
2
Dosage Form
-
Strength
15MG;0.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE
Application Number
17503
Product Number
2
Dosage Form
-
Strength
15MG;0.2MG **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
COMBIPRES
Product Number
3
Dosage Form
-
Strength
15MG;0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-04-10
Active Ingredient
CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE
Application Number
17503
Product Number
3
Dosage Form
-
Strength
15MG;0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-04-10
Regulatory Status
Discontinued
Drug Name
COMBIVENT
Product Number
1
Dosage Form
-
Strength
EQ 0.09MG BASE/INH;0.018MG/INH
Approval Date
1996-10-24
Active Ingredient
ALBUTEROL SULFATE; IPRATROPIUM BROMIDE
Application Number
20291
Product Number
1
Dosage Form
-
Strength
EQ 0.09MG BASE/INH;0.018MG/INH
Approval Date
1996-10-24
Regulatory Status
Discontinued
Drug Name
IV PERSANTINE
Product Number
1
Dosage Form
-
Strength
5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1990-12-13
Active Ingredient
DIPYRIDAMOLE
Application Number
19817
Product Number
1
Dosage Form
-
Strength
5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1990-12-13
Regulatory Status
Discontinued
Drug Name
MEXITIL
Product Number
2
Dosage Form
-
Strength
150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-12-30
Active Ingredient
MEXILETINE HYDROCHLORIDE
Application Number
18873
Product Number
2
Dosage Form
-
Strength
150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-12-30
Regulatory Status
Discontinued
Drug Name
MEXITIL
Product Number
3
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-12-30
Active Ingredient
MEXILETINE HYDROCHLORIDE
Application Number
18873
Product Number
3
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-12-30
Regulatory Status
Discontinued
Drug Name
MEXITIL
Product Number
4
Dosage Form
-
Strength
250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-12-30
Active Ingredient
MEXILETINE HYDROCHLORIDE
Application Number
18873
Product Number
4
Dosage Form
-
Strength
250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-12-30
Regulatory Status
Discontinued
Drug Name
MICARDIS
Product Number
1
Dosage Form
-
Strength
40MG
Approval Date
1998-11-10
Active Ingredient
TELMISARTAN
Application Number
20850
Product Number
1
Dosage Form
-
Strength
40MG
Approval Date
1998-11-10
Regulatory Status
Discontinued
Drug Name
MICARDIS
Product Number
2
Dosage Form
-
Strength
80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1998-11-10
Active Ingredient
TELMISARTAN
Application Number
20850
Product Number
2
Dosage Form
-
Strength
80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1998-11-10
Regulatory Status
Discontinued
Drug Name
MICARDIS
Product Number
3
Dosage Form
-
Strength
20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2000-04-04
Active Ingredient
TELMISARTAN
Application Number
20850
Product Number
3
Dosage Form
-
Strength
20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2000-04-04
Regulatory Status
Discontinued
Drug Name
MIRAPEX
Product Number
1
Dosage Form
-
Strength
0.125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-07-01
Active Ingredient
PRAMIPEXOLE DIHYDROCHLORIDE
Application Number
20667
Product Number
1
Dosage Form
-
Strength
0.125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-07-01
Regulatory Status
Discontinued
Drug Name
MIRAPEX
Product Number
2
Dosage Form
-
Strength
0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-07-01
Active Ingredient
PRAMIPEXOLE DIHYDROCHLORIDE
Application Number
20667
Product Number
2
Dosage Form
-
Strength
0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-07-01
Regulatory Status
Discontinued
Drug Name
MIRAPEX
Product Number
3
Dosage Form
-
Strength
1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-07-01
Active Ingredient
PRAMIPEXOLE DIHYDROCHLORIDE
Application Number
20667
Product Number
3
Dosage Form
-
Strength
1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-07-01
Regulatory Status
Discontinued
Drug Name
MIRAPEX
Product Number
4
Dosage Form
-
Strength
1.25MG
Approval Date
1997-07-01
Active Ingredient
PRAMIPEXOLE DIHYDROCHLORIDE
Application Number
20667
Product Number
4
Dosage Form
-
Strength
1.25MG
Approval Date
1997-07-01
Regulatory Status
Discontinued
Drug Name
MIRAPEX
Product Number
5
Dosage Form
-
Strength
1.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-07-01
Active Ingredient
PRAMIPEXOLE DIHYDROCHLORIDE
Application Number
20667
Product Number
5
Dosage Form
-
Strength
1.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-07-01
Regulatory Status
Discontinued
Drug Name
MIRAPEX
Product Number
6
Dosage Form
-
Strength
0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1998-02-12
Active Ingredient
PRAMIPEXOLE DIHYDROCHLORIDE
Application Number
20667
Product Number
6
Dosage Form
-
Strength
0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1998-02-12
Regulatory Status
Discontinued
Drug Name
MIRAPEX
Product Number
7
Dosage Form
-
Strength
0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2007-07-30
Active Ingredient
PRAMIPEXOLE DIHYDROCHLORIDE
Application Number
20667
Product Number
7
Dosage Form
-
Strength
0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2007-07-30
Regulatory Status
Discontinued
Drug Name
MIRAPEX ER
Product Number
1
Dosage Form
-
Strength
0.375MG
Approval Date
2010-02-19
Active Ingredient
PRAMIPEXOLE DIHYDROCHLORIDE
Application Number
22421
Product Number
1
Dosage Form
-
Strength
0.375MG
Approval Date
2010-02-19
Regulatory Status
Discontinued
Drug Name
MIRAPEX ER
Product Number
2
Dosage Form
-
Strength
0.75MG
Approval Date
2010-02-19
Active Ingredient
PRAMIPEXOLE DIHYDROCHLORIDE
Application Number
22421
Product Number
2
Dosage Form
-
Strength
0.75MG
Approval Date
2010-02-19
Regulatory Status
Discontinued
Drug Name
MIRAPEX ER
Product Number
3
Dosage Form
-
Strength
1.5MG
Approval Date
2010-02-19
Active Ingredient
PRAMIPEXOLE DIHYDROCHLORIDE
Application Number
22421
Product Number
3
Dosage Form
-
Strength
1.5MG
Approval Date
2010-02-19
Regulatory Status
Discontinued
Drug Name
MIRAPEX ER
Product Number
4
Dosage Form
-
Strength
3MG
Approval Date
2010-02-19
Active Ingredient
PRAMIPEXOLE DIHYDROCHLORIDE
Application Number
22421
Product Number
4
Dosage Form
-
Strength
3MG
Approval Date
2010-02-19
Regulatory Status
Discontinued
Drug Name
MIRAPEX ER
Product Number
5
Dosage Form
-
Strength
4.5MG
Approval Date
2010-02-19
Active Ingredient
PRAMIPEXOLE DIHYDROCHLORIDE
Application Number
22421
Product Number
5
Dosage Form
-
Strength
4.5MG
Approval Date
2010-02-19
Regulatory Status
Discontinued
Drug Name
MIRAPEX ER
Product Number
6
Dosage Form
-
Strength
2.25MG
Approval Date
2011-06-17
Active Ingredient
PRAMIPEXOLE DIHYDROCHLORIDE
Application Number
22421
Product Number
6
Dosage Form
-
Strength
2.25MG
Approval Date
2011-06-17
Regulatory Status
Discontinued
Drug Name
MIRAPEX ER
Product Number
7
Dosage Form
-
Strength
3.75MG
Approval Date
2011-06-17
Active Ingredient
PRAMIPEXOLE DIHYDROCHLORIDE
Application Number
22421
Product Number
7
Dosage Form
-
Strength
3.75MG
Approval Date
2011-06-17
Regulatory Status
Discontinued
Drug Name
MOBIC
Product Number
1
Dosage Form
-
Strength
7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2000-04-13
Active Ingredient
MELOXICAM
Application Number
20938
Product Number
1
Dosage Form
-
Strength
7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2000-04-13
Regulatory Status
Discontinued
Drug Name
MOBIC
Product Number
2
Dosage Form
-
Strength
15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2000-08-23
Active Ingredient
MELOXICAM
Application Number
20938
Product Number
2
Dosage Form
-
Strength
15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2000-08-23
Regulatory Status
Discontinued
Drug Name
PERSANTINE
Product Number
3
Dosage Form
-
Strength
25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1986-12-22
Active Ingredient
DIPYRIDAMOLE
Application Number
12836
Product Number
3
Dosage Form
-
Strength
25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1986-12-22
Regulatory Status
Discontinued
Drug Name
PERSANTINE
Product Number
4
Dosage Form
-
Strength
50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-02-06
Active Ingredient
DIPYRIDAMOLE
Application Number
12836
Product Number
4
Dosage Form
-
Strength
50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-02-06
Regulatory Status
Discontinued
Drug Name
PERSANTINE
Product Number
5
Dosage Form
-
Strength
75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-02-06
Active Ingredient
DIPYRIDAMOLE
Application Number
12836
Product Number
5
Dosage Form
-
Strength
75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1987-02-06
Regulatory Status
Discontinued
Drug Name
PRELUDIN
Product Number
5
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
PHENMETRAZINE HYDROCHLORIDE
Application Number
10460
Product Number
5
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PRELUDIN
Product Number
3
Dosage Form
-
Strength
75MG
Approval Date
1982-01-01
Active Ingredient
PHENMETRAZINE HYDROCHLORIDE
Application Number
11752
Product Number
3
Dosage Form
-
Strength
75MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PRELUDIN
Product Number
4
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Active Ingredient
PHENMETRAZINE HYDROCHLORIDE
Application Number
11752
Product Number
4
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE
Approval Date
1997-08-29
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
74662
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE
Approval Date
1997-08-29
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 300MG BASE
Approval Date
1997-08-29
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
74662
Product Number
2
Dosage Form
-
Strength
EQ 300MG BASE
Approval Date
1997-08-29
Regulatory Status
Discontinued
Drug Name
TWYNSTA
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2009-10-16
Active Ingredient
AMLODIPINE BESYLATE; TELMISARTAN
Application Number
22401
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2009-10-16
Regulatory Status
Discontinued
Drug Name
TWYNSTA
Product Number
2
Dosage Form
-
Strength
EQ 10MG BASE;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2009-10-16
Active Ingredient
AMLODIPINE BESYLATE; TELMISARTAN
Application Number
22401
Product Number
2
Dosage Form
-
Strength
EQ 10MG BASE;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2009-10-16
Regulatory Status
Discontinued
Drug Name
TWYNSTA
Product Number
3
Dosage Form
-
Strength
EQ 5MG BASE;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2009-10-16
Active Ingredient
AMLODIPINE BESYLATE; TELMISARTAN
Application Number
22401
Product Number
3
Dosage Form
-
Strength
EQ 5MG BASE;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2009-10-16
Regulatory Status
Discontinued
Drug Name
TWYNSTA
Product Number
4
Dosage Form
-
Strength
EQ 10MG BASE;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2009-10-16
Active Ingredient
AMLODIPINE BESYLATE; TELMISARTAN
Application Number
22401
Product Number
4
Dosage Form
-
Strength
EQ 10MG BASE;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2009-10-16
Regulatory Status
Discontinued
Drug Name
VIRAMUNE
Product Number
1
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1996-06-21
Active Ingredient
NEVIRAPINE
Application Number
20636
Product Number
1
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1996-06-21
Regulatory Status
Discontinued
Drug Name
VIRAMUNE
Product Number
1
Dosage Form
-
Strength
50MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1998-09-11
Active Ingredient
NEVIRAPINE
Application Number
20933
Product Number
1
Dosage Form
-
Strength
50MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1998-09-11
Regulatory Status
Discontinued
Drug Name
VIRAMUNE XR
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
2011-03-25
Active Ingredient
NEVIRAPINE
Application Number
201152
Product Number
1
Dosage Form
-
Strength
400MG
Approval Date
2011-03-25
Regulatory Status
Discontinued
Drug Name
VIRAMUNE XR
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
2012-11-08
Active Ingredient
NEVIRAPINE
Application Number
201152
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
2012-11-08
Regulatory Status
Discontinued
Drug Status Breakdown
59 total- Discontinued
Official Source
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Drug Name
AGGRENOX
Application Number
20884
Product Number
1
Active Ingredient
ASPIRIN; DIPYRIDAMOLE
Dosage Form
-
Strength
25MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
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