Bausch Health Discontinued
FDA Approved Drugs
Bausch Health 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 79
- Latest Approval Date Apr 15, 2011
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Overview
Social Profiles
Company Snapshot
Bausch Health Discontinued
2150 St. Elzear Blvd. WestLaval, Quebec H7L 4A8
Canada
www.bauschhealth.com/ View on MapFDA Approved Drug Records ( 79 records )
Drug Name
8-MOP
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Active Ingredient
METHOXSALEN
Application Number
9048
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
1982-01-01
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Application Number
85896
Product Number
1
Dosage Form
-
Strength
300MG;30MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
AMINOPHYLLINE
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1982-01-01
Active Ingredient
AMINOPHYLLINE
Application Number
84563
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ANDROID 10
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Active Ingredient
METHYLTESTOSTERONE
Application Number
86450
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ANDROID 5
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Active Ingredient
METHYLTESTOSTERONE
Application Number
87222
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ANDROID-F
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Active Ingredient
FLUOXYMESTERONE
Application Number
87196
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BENDOPA
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1982-01-01
Active Ingredient
LEVODOPA
Application Number
16948
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BENDOPA
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Active Ingredient
LEVODOPA
Application Number
16948
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BENDOPA
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Active Ingredient
LEVODOPA
Application Number
16948
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BENOQUIN
Product Number
3
Dosage Form
-
Strength
20%
Approval Date
1982-01-01
Active Ingredient
MONOBENZONE
Application Number
8173
Product Number
3
Dosage Form
-
Strength
20%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BONTRIL
Product Number
1
Dosage Form
-
Strength
105MG
Approval Date
1982-09-21
Active Ingredient
PHENDIMETRAZINE TARTRATE
Application Number
88021
Product Number
1
Dosage Form
-
Strength
105MG
Approval Date
1982-09-21
Regulatory Status
Discontinued
Drug Name
CAPITAL AND CODEINE
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
1982-01-01
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Application Number
86024
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DALMANE
Product Number
1
Dosage Form
-
Strength
15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
FLURAZEPAM HYDROCHLORIDE
Application Number
16721
Product Number
1
Dosage Form
-
Strength
15MG **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
DALMANE
Product Number
2
Dosage Form
-
Strength
30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
FLURAZEPAM HYDROCHLORIDE
Application Number
16721
Product Number
2
Dosage Form
-
Strength
30MG **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
DERMATOP
Product Number
1
Dosage Form
-
Strength
0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-09-23
Active Ingredient
PREDNICARBATE
Application Number
19568
Product Number
1
Dosage Form
-
Strength
0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-09-23
Regulatory Status
Discontinued
Drug Name
DERMATOP E EMOLLIENT
Product Number
1
Dosage Form
-
Strength
0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-10-29
Active Ingredient
PREDNICARBATE
Application Number
20279
Product Number
1
Dosage Form
-
Strength
0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-10-29
Regulatory Status
Discontinued
Drug Name
DIPHENHYDRAMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Active Ingredient
DIPHENHYDRAMINE HYDROCHLORIDE
Application Number
80592
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DIPHENHYDRAMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
DIPHENHYDRAMINE HYDROCHLORIDE
Application Number
80596
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
Product Number
1
Dosage Form
-
Strength
0.025MG;2.5MG
Approval Date
1982-02-16
Active Ingredient
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Application Number
87195
Product Number
1
Dosage Form
-
Strength
0.025MG;2.5MG
Approval Date
1982-02-16
Regulatory Status
Discontinued
Drug Name
ELDECORT
Product Number
1
Dosage Form
-
Strength
1%
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE
Application Number
80459
Product Number
1
Dosage Form
-
Strength
1%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ELDECORT
Product Number
1
Dosage Form
-
Strength
2.5%
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE
Application Number
84055
Product Number
1
Dosage Form
-
Strength
2.5%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
FLUOXYMESTERONE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1983-05-05
Active Ingredient
FLUOXYMESTERONE
Application Number
88221
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1983-05-05
Regulatory Status
Discontinued
Drug Name
FOLIC ACID
Product Number
1
Dosage Form
-
Strength
1MG
Approval Date
1982-01-01
Active Ingredient
FOLIC ACID
Application Number
80903
Product Number
1
Dosage Form
-
Strength
1MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
GRIFULVIN V
Product Number
1
Dosage Form
-
Strength
125MG
Approval Date
1982-01-01
Active Ingredient
GRISEOFULVIN, MICROCRYSTALLINE
Application Number
62279
Product Number
1
Dosage Form
-
Strength
125MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
GRIFULVIN V
Product Number
2
Dosage Form
-
Strength
250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
GRISEOFULVIN, MICROCRYSTALLINE
Application Number
62279
Product Number
2
Dosage Form
-
Strength
250MG **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
GRIFULVIN V
Product Number
3
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Active Ingredient
GRISEOFULVIN, MICROSIZE
Application Number
62279
Product Number
3
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
GRIFULVIN V
Product Number
1
Dosage Form
-
Strength
125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-01-26
Active Ingredient
GRISEOFULVIN, MICROSIZE
Application Number
62483
Product Number
1
Dosage Form
-
Strength
125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-01-26
Regulatory Status
Discontinued
Drug Name
HYTONE
Product Number
3
Dosage Form
-
Strength
1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE
Application Number
80472
Product Number
3
Dosage Form
-
Strength
1% **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
HYTONE
Product Number
4
Dosage Form
-
Strength
2.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE
Application Number
80472
Product Number
4
Dosage Form
-
Strength
2.5% **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
HYTONE
Product Number
3
Dosage Form
-
Strength
1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE
Application Number
80473
Product Number
3
Dosage Form
-
Strength
1% **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
HYTONE
Product Number
4
Dosage Form
-
Strength
2.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-11-30
Active Ingredient
HYDROCORTISONE
Application Number
80473
Product Number
4
Dosage Form
-
Strength
2.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-11-30
Regulatory Status
Discontinued
Drug Name
LEVO-DROMORAN
Product Number
1
Dosage Form
-
Strength
2MG/ML
Approval Date
1991-12-19
Active Ingredient
LEVORPHANOL TARTRATE
Application Number
8719
Product Number
1
Dosage Form
-
Strength
2MG/ML
Approval Date
1991-12-19
Regulatory Status
Discontinued
Drug Name
LEVO-DROMORAN
Product Number
1
Dosage Form
-
Strength
2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-12-19
Active Ingredient
LEVORPHANOL TARTRATE
Application Number
8720
Product Number
1
Dosage Form
-
Strength
2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-12-19
Regulatory Status
Discontinued
Drug Name
LIBRELEASE
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
1983-09-12
Active Ingredient
CHLORDIAZEPOXIDE
Application Number
17813
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
1983-09-12
Regulatory Status
Discontinued
Drug Name
LIBRITABS
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Active Ingredient
CHLORDIAZEPOXIDE
Application Number
85481
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
LIBRITABS
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Active Ingredient
CHLORDIAZEPOXIDE
Application Number
85482
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
LIBRITABS
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
CHLORDIAZEPOXIDE
Application Number
85488
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
LIBRIUM
Product Number
1
Dosage Form
-
Strength
10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CHLORDIAZEPOXIDE HYDROCHLORIDE
Application Number
12249
Product Number
1
Dosage Form
-
Strength
10MG **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
LIBRIUM
Product Number
2
Dosage Form
-
Strength
5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CHLORDIAZEPOXIDE HYDROCHLORIDE
Application Number
12249
Product Number
2
Dosage Form
-
Strength
5MG **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
LIBRIUM
Product Number
3
Dosage Form
-
Strength
25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CHLORDIAZEPOXIDE HYDROCHLORIDE
Application Number
12249
Product Number
3
Dosage Form
-
Strength
25MG **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
MEPROBAMATE
Product Number
5
Dosage Form
-
Strength
400MG
Approval Date
1982-01-01
Active Ingredient
MEPROBAMATE
Application Number
15139
Product Number
5
Dosage Form
-
Strength
400MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MEPROBAMATE
Product Number
6
Dosage Form
-
Strength
200MG
Approval Date
1982-01-01
Active Ingredient
MEPROBAMATE
Application Number
15139
Product Number
6
Dosage Form
-
Strength
200MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MINITRAN
Product Number
1
Dosage Form
-
Strength
0.1MG/HR
Approval Date
1996-08-30
Active Ingredient
NITROGLYCERIN
Application Number
89771
Product Number
1
Dosage Form
-
Strength
0.1MG/HR
Approval Date
1996-08-30
Regulatory Status
Discontinued
Drug Name
MINITRAN
Product Number
1
Dosage Form
-
Strength
0.2MG/HR
Approval Date
1996-08-30
Active Ingredient
NITROGLYCERIN
Application Number
89772
Product Number
1
Dosage Form
-
Strength
0.2MG/HR
Approval Date
1996-08-30
Regulatory Status
Discontinued
Drug Name
MINITRAN
Product Number
1
Dosage Form
-
Strength
0.6MG/HR
Approval Date
1996-08-30
Active Ingredient
NITROGLYCERIN
Application Number
89774
Product Number
1
Dosage Form
-
Strength
0.6MG/HR
Approval Date
1996-08-30
Regulatory Status
Discontinued
Drug Name
NITROPRESS
Product Number
1
Dosage Form
-
Strength
25MG/ML
Approval Date
1988-08-01
Active Ingredient
SODIUM NITROPRUSSIDE
Application Number
71961
Product Number
1
Dosage Form
-
Strength
25MG/ML
Approval Date
1988-08-01
Regulatory Status
Discontinued
Drug Name
OXSORALEN
Product Number
2
Dosage Form
-
Strength
1%
Approval Date
1982-01-01
Active Ingredient
METHOXSALEN
Application Number
9048
Product Number
2
Dosage Form
-
Strength
1%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PENLAC
Product Number
1
Dosage Form
-
Strength
8% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1999-12-17
Active Ingredient
CICLOPIROX
Application Number
21022
Product Number
1
Dosage Form
-
Strength
8% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1999-12-17
Regulatory Status
Discontinued
Drug Name
PERMAX
Product Number
1
Dosage Form
-
Strength
EQ 0.05MG BASE
Approval Date
1988-12-30
Active Ingredient
PERGOLIDE MESYLATE
Application Number
19385
Product Number
1
Dosage Form
-
Strength
EQ 0.05MG BASE
Approval Date
1988-12-30
Regulatory Status
Discontinued
Drug Name
PERMAX
Product Number
2
Dosage Form
-
Strength
EQ 0.25MG BASE
Approval Date
1988-12-30
Active Ingredient
PERGOLIDE MESYLATE
Application Number
19385
Product Number
2
Dosage Form
-
Strength
EQ 0.25MG BASE
Approval Date
1988-12-30
Regulatory Status
Discontinued
Drug Name
PERMAX
Product Number
3
Dosage Form
-
Strength
EQ 1MG BASE
Approval Date
1988-12-30
Active Ingredient
PERGOLIDE MESYLATE
Application Number
19385
Product Number
3
Dosage Form
-
Strength
EQ 1MG BASE
Approval Date
1988-12-30
Regulatory Status
Discontinued
Drug Name
PHRENILIN
Product Number
1
Dosage Form
-
Strength
325MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-06-19
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Application Number
87811
Product Number
1
Dosage Form
-
Strength
325MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-06-19
Regulatory Status
Discontinued
Drug Name
PHRENILIN FORTE
Product Number
1
Dosage Form
-
Strength
650MG;50MG
Approval Date
1985-06-19
Active Ingredient
ACETAMINOPHEN; BUTALBITAL
Application Number
88831
Product Number
1
Dosage Form
-
Strength
650MG;50MG
Approval Date
1985-06-19
Regulatory Status
Discontinued
Drug Name
PHRENILIN WITH CAFFEINE AND CODEINE
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG;30MG
Approval Date
2001-08-22
Active Ingredient
ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
Application Number
74911
Product Number
1
Dosage Form
-
Strength
325MG;50MG;40MG;30MG
Approval Date
2001-08-22
Regulatory Status
Discontinued
Drug Name
PREDNISOLONE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Active Ingredient
PREDNISOLONE
Application Number
80236
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PREDNISONE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Active Ingredient
PREDNISONE
Application Number
80237
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
65MG
Approval Date
1982-01-01
Active Ingredient
PROPOXYPHENE HYDROCHLORIDE
Application Number
80783
Product Number
1
Dosage Form
-
Strength
65MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
QUINIDINE SULFATE
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1982-01-01
Active Ingredient
QUINIDINE SULFATE
Application Number
83393
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
RAUWOLFIA SERPENTINA
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Active Ingredient
RAUWOLFIA SERPENTINA ROOT
Application Number
9668
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
RAUWOLFIA SERPENTINA
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Active Ingredient
RAUWOLFIA SERPENTINA ROOT
Application Number
9668
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
RENOVA
Product Number
1
Dosage Form
-
Strength
0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-12-29
Active Ingredient
TRETINOIN
Application Number
19963
Product Number
1
Dosage Form
-
Strength
0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-12-29
Regulatory Status
Discontinued
Drug Name
RESERPINE
Product Number
1
Dosage Form
-
Strength
0.1MG
Approval Date
1982-01-01
Active Ingredient
RESERPINE
Application Number
9667
Product Number
1
Dosage Form
-
Strength
0.1MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
RESERPINE
Product Number
2
Dosage Form
-
Strength
0.25MG
Approval Date
1982-01-01
Active Ingredient
RESERPINE
Application Number
9667
Product Number
2
Dosage Form
-
Strength
0.25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
RETIN-A
Product Number
1
Dosage Form
-
Strength
0.05%
Approval Date
1982-01-01
Active Ingredient
TRETINOIN
Application Number
16921
Product Number
1
Dosage Form
-
Strength
0.05%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
RETIN-A
Product Number
2
Dosage Form
-
Strength
0.05%
Approval Date
1982-01-01
Active Ingredient
TRETINOIN
Application Number
16921
Product Number
2
Dosage Form
-
Strength
0.05%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
SECOBARBITAL SODIUM
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Active Ingredient
SECOBARBITAL SODIUM
Application Number
85477
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
SECONAL SODIUM
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1983-10-03
Active Ingredient
SECOBARBITAL SODIUM
Application Number
86101
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1983-10-03
Regulatory Status
Discontinued
Drug Name
SECONAL SODIUM
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
1983-10-03
Active Ingredient
SECOBARBITAL SODIUM
Application Number
86101
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
1983-10-03
Regulatory Status
Discontinued
Drug Name
SODIUM PENTOBARBITAL
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Active Ingredient
PENTOBARBITAL SODIUM
Application Number
83264
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
SULFISOXAZOLE
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Active Ingredient
SULFISOXAZOLE
Application Number
80268
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TETRACYCLINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1982-01-01
Active Ingredient
TETRACYCLINE HYDROCHLORIDE
Application Number
60471
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TETRACYCLINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Active Ingredient
TETRACYCLINE HYDROCHLORIDE
Application Number
60471
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TRISORALEN
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Active Ingredient
TRIOXSALEN
Application Number
12697
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ULTRAM ER
Product Number
1
Dosage Form
-
Strength
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2005-09-08
Active Ingredient
TRAMADOL HYDROCHLORIDE
Application Number
21692
Product Number
1
Dosage Form
-
Strength
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2005-09-08
Regulatory Status
Discontinued
Drug Name
ULTRAM ER
Product Number
2
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2005-09-08
Active Ingredient
TRAMADOL HYDROCHLORIDE
Application Number
21692
Product Number
2
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2005-09-08
Regulatory Status
Discontinued
Drug Name
ULTRAM ER
Product Number
3
Dosage Form
-
Strength
300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2005-09-08
Active Ingredient
TRAMADOL HYDROCHLORIDE
Application Number
21692
Product Number
3
Dosage Form
-
Strength
300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2005-09-08
Regulatory Status
Discontinued
Drug Name
VENLAFAXINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 37.5MG BASE
Approval Date
2011-04-15
Active Ingredient
VENLAFAXINE HYDROCHLORIDE
Application Number
90071
Product Number
1
Dosage Form
-
Strength
EQ 37.5MG BASE
Approval Date
2011-04-15
Regulatory Status
Discontinued
Drug Name
VENLAFAXINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
2011-04-15
Active Ingredient
VENLAFAXINE HYDROCHLORIDE
Application Number
90071
Product Number
2
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
2011-04-15
Regulatory Status
Discontinued
Drug Name
VENLAFAXINE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
EQ 150MG BASE
Approval Date
2011-04-15
Active Ingredient
VENLAFAXINE HYDROCHLORIDE
Application Number
90071
Product Number
3
Dosage Form
-
Strength
EQ 150MG BASE
Approval Date
2011-04-15
Regulatory Status
Discontinued
Drug Status Breakdown
79 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
8-MOP
Application Number
9048
Product Number
1
Active Ingredient
METHOXSALEN
Dosage Form
-
Strength
10MG
FDA Approved Drug Data
Approved drug product information
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