Fougera Pharmaceuticals Inc. Discontinued
FDA Approved Drugs
Fougera Pharmaceuticals Inc. 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 33
- Latest Approval Date Jan 28, 2019
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Snapshot
FDA Approved Drug Records ( 33 records )
Drug Name
ACLOVATE
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0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
1982-12-14
Active Ingredient
ALCLOMETASONE DIPROPIONATE
Application Number
18702
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0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
1982-12-14
Regulatory Status
Discontinued
Drug Name
ACLOVATE
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0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
1982-12-14
Active Ingredient
ALCLOMETASONE DIPROPIONATE
Application Number
18707
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0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
1982-12-14
Regulatory Status
Discontinued
Drug Name
C-SOLVE-2
Product Number
1
Dosage Form
-
Strength
2%
Approval Date
1985-07-03
Active Ingredient
ERYTHROMYCIN
Application Number
62468
Product Number
1
Dosage Form
-
Strength
2%
Approval Date
1985-07-03
Regulatory Status
Discontinued
Drug Name
CARMOL HC
Product Number
1
Dosage Form
-
Strength
1%
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE ACETATE
Application Number
80505
Product Number
1
Dosage Form
-
Strength
1%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CLINDAMYCIN PHOSPHATE
Product Number
1
Dosage Form
-
Strength
EQ 1% BASE
Approval Date
2006-02-14
Active Ingredient
CLINDAMYCIN PHOSPHATE
Application Number
65254
Product Number
1
Dosage Form
-
Strength
EQ 1% BASE
Approval Date
2006-02-14
Regulatory Status
Discontinued
Drug Name
CUTIVATE
Product Number
1
Dosage Form
-
Strength
0.005% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1990-12-14
Active Ingredient
FLUTICASONE PROPIONATE
Application Number
19957
Product Number
1
Dosage Form
-
Strength
0.005% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1990-12-14
Regulatory Status
Discontinued
Drug Name
CUTIVATE
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
1990-12-18
Active Ingredient
FLUTICASONE PROPIONATE
Application Number
19958
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
1990-12-18
Regulatory Status
Discontinued
Drug Name
CUTIVATE
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
2005-03-31
Active Ingredient
FLUTICASONE PROPIONATE
Application Number
21152
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
2005-03-31
Regulatory Status
Discontinued
Drug Name
ERYTHROMYCIN
Product Number
1
Dosage Form
-
Strength
2%
Approval Date
1997-09-30
Active Ingredient
ERYTHROMYCIN
Application Number
64187
Product Number
1
Dosage Form
-
Strength
2%
Approval Date
1997-09-30
Regulatory Status
Discontinued
Drug Name
ERYTHROMYCIN
Product Number
1
Dosage Form
-
Strength
2%
Approval Date
2006-07-25
Active Ingredient
ERYTHROMYCIN
Application Number
65320
Product Number
1
Dosage Form
-
Strength
2%
Approval Date
2006-07-25
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE
Product Number
1
Dosage Form
-
Strength
EQ 0.1% BASE
Approval Date
1984-07-05
Active Ingredient
GENTAMICIN SULFATE
Application Number
62531
Product Number
1
Dosage Form
-
Strength
EQ 0.1% BASE
Approval Date
1984-07-05
Regulatory Status
Discontinued
Drug Name
HALOBETASOL PROPIONATE
Product Number
1
Dosage Form
-
Strength
0.05%
Approval Date
2004-12-16
Active Ingredient
HALOBETASOL PROPIONATE
Application Number
76903
Product Number
1
Dosage Form
-
Strength
0.05%
Approval Date
2004-12-16
Regulatory Status
Discontinued
Drug Name
HYDROCORTISONE
Product Number
1
Dosage Form
-
Strength
2.5%
Approval Date
2000-07-25
Active Ingredient
HYDROCORTISONE
Application Number
40351
Product Number
1
Dosage Form
-
Strength
2.5%
Approval Date
2000-07-25
Regulatory Status
Discontinued
Drug Name
HYDROCORTISONE VALERATE
Product Number
1
Dosage Form
-
Strength
0.2%
Approval Date
2001-07-31
Active Ingredient
HYDROCORTISONE VALERATE
Application Number
75085
Product Number
1
Dosage Form
-
Strength
0.2%
Approval Date
2001-07-31
Regulatory Status
Discontinued
Drug Name
MOMETASONE FUROATE
Product Number
1
Dosage Form
-
Strength
0.1%
Approval Date
2005-04-08
Active Ingredient
MOMETASONE FUROATE
Application Number
76171
Product Number
1
Dosage Form
-
Strength
0.1%
Approval Date
2005-04-08
Regulatory Status
Discontinued
Drug Name
NEOMYCIN SULFATE-TRIAMCINOLONE ACETONIDE
Product Number
1
Dosage Form
-
Strength
EQ 3.5MG BASE/GM;0.1%
Approval Date
1986-07-21
Active Ingredient
NEOMYCIN SULFATE; TRIAMCINOLONE ACETONIDE
Application Number
62600
Product Number
1
Dosage Form
-
Strength
EQ 3.5MG BASE/GM;0.1%
Approval Date
1986-07-21
Regulatory Status
Discontinued
Drug Name
NEOMYCIN SULFATE-TRIAMCINOLONE ACETONIDE
Product Number
1
Dosage Form
-
Strength
EQ 3.5MG BASE/GM;0.1%
Approval Date
1986-05-23
Active Ingredient
NEOMYCIN SULFATE; TRIAMCINOLONE ACETONIDE
Application Number
62608
Product Number
1
Dosage Form
-
Strength
EQ 3.5MG BASE/GM;0.1%
Approval Date
1986-05-23
Regulatory Status
Discontinued
Drug Name
NYSTATIN
Product Number
1
Dosage Form
-
Strength
100,000 UNITS
Approval Date
1983-11-09
Active Ingredient
NYSTATIN
Application Number
62459
Product Number
1
Dosage Form
-
Strength
100,000 UNITS
Approval Date
1983-11-09
Regulatory Status
Discontinued
Drug Name
PAMINE
Product Number
1
Dosage Form
-
Strength
2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
METHSCOPOLAMINE BROMIDE
Application Number
8848
Product Number
1
Dosage Form
-
Strength
2.5MG **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
PAMINE FORTE
Product Number
2
Dosage Form
-
Strength
5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-03-25
Active Ingredient
METHSCOPOLAMINE BROMIDE
Application Number
8848
Product Number
2
Dosage Form
-
Strength
5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-03-25
Regulatory Status
Discontinued
Drug Name
PREDNICARBATE
Product Number
1
Dosage Form
-
Strength
0.1%
Approval Date
2006-09-19
Active Ingredient
PREDNICARBATE
Application Number
77287
Product Number
1
Dosage Form
-
Strength
0.1%
Approval Date
2006-09-19
Regulatory Status
Discontinued
Drug Name
SOLARAZE
Product Number
1
Dosage Form
-
Strength
3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2000-10-16
Active Ingredient
DICLOFENAC SODIUM
Application Number
21005
Product Number
1
Dosage Form
-
Strength
3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2000-10-16
Regulatory Status
Discontinued
Drug Name
TAZAROTENE
Product Number
1
Dosage Form
-
Strength
0.1%
Approval Date
2019-01-28
Active Ingredient
TAZAROTENE
Application Number
211175
Product Number
1
Dosage Form
-
Strength
0.1%
Approval Date
2019-01-28
Regulatory Status
Discontinued
Drug Name
TEMOVATE
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
1985-12-27
Active Ingredient
CLOBETASOL PROPIONATE
Application Number
19322
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
1985-12-27
Regulatory Status
Discontinued
Drug Name
TEMOVATE
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
1985-12-27
Active Ingredient
CLOBETASOL PROPIONATE
Application Number
19323
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
1985-12-27
Regulatory Status
Discontinued
Drug Name
TEMOVATE
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
1990-02-22
Active Ingredient
CLOBETASOL PROPIONATE
Application Number
19966
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
1990-02-22
Regulatory Status
Discontinued
Drug Name
TEMOVATE
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
1994-04-29
Active Ingredient
CLOBETASOL PROPIONATE
Application Number
20337
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
1994-04-29
Regulatory Status
Discontinued
Drug Name
TEMOVATE E
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
1994-06-17
Active Ingredient
CLOBETASOL PROPIONATE
Application Number
20340
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
1994-06-17
Regulatory Status
Discontinued
Drug Name
TERCONAZOLE
Product Number
1
Dosage Form
-
Strength
80MG
Approval Date
2006-07-12
Active Ingredient
TERCONAZOLE
Application Number
76850
Product Number
1
Dosage Form
-
Strength
80MG
Approval Date
2006-07-12
Regulatory Status
Discontinued
Drug Name
TIMOLOL MALEATE
Product Number
1
Dosage Form
-
Strength
EQ 0.25% BASE
Approval Date
1997-03-25
Active Ingredient
TIMOLOL MALEATE
Application Number
74667
Product Number
1
Dosage Form
-
Strength
EQ 0.25% BASE
Approval Date
1997-03-25
Regulatory Status
Discontinued
Drug Name
TIMOLOL MALEATE
Product Number
1
Dosage Form
-
Strength
EQ 0.5% BASE
Approval Date
1997-03-25
Active Ingredient
TIMOLOL MALEATE
Application Number
74668
Product Number
1
Dosage Form
-
Strength
EQ 0.5% BASE
Approval Date
1997-03-25
Regulatory Status
Discontinued
Drug Name
TRIPLE SULFA
Product Number
1
Dosage Form
-
Strength
3.7%;2.86%;3.42%
Approval Date
1982-01-01
Active Ingredient
TRIPLE SULFA (SULFABENZAMIDE;SULFACETAMIDE;SULFATHIAZOLE)
Application Number
86424
Product Number
1
Dosage Form
-
Strength
3.7%;2.86%;3.42%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TRIPLE SULFA
Product Number
1
Dosage Form
-
Strength
184MG;143.75MG;172.5MG
Approval Date
1985-01-03
Active Ingredient
TRIPLE SULFA (SULFABENZAMIDE;SULFACETAMIDE;SULFATHIAZOLE)
Application Number
88463
Product Number
1
Dosage Form
-
Strength
184MG;143.75MG;172.5MG
Approval Date
1985-01-03
Regulatory Status
Discontinued
Drug Status Breakdown
33 total- Discontinued
Official Source
FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.
Visit FDA Orange BookFDA Approved Drug Record Details Preview
Explore important FDA approved drug information available in the records above.
Drug Name
ACLOVATE
Application Number
18702
Product Number
1
Active Ingredient
ALCLOMETASONE DIPROPIONATE
Dosage Form
-
Strength
0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
FDA Approved Drug Data
Approved drug product information
Regular Updates
Data maintained from official sources
Structured Database
Searchable pharmaceutical data
Reliable Data
Organized FDA drug records
Create a New Buying Request
Fields marked with * are mandatory.