PHARM ASSOC Discontinued
FDA Approved Drugs
PHARM ASSOC 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 36
- Latest Approval Date Mar 11, 2020
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Snapshot
FDA Approved Drug Records ( 36 records )
Drug Name
BROMPHENIRAMINE MALEATE
Product Number
1
Dosage Form
-
Strength
2MG/5ML
Approval Date
1982-01-01
Active Ingredient
BROMPHENIRAMINE MALEATE
Application Number
87517
Product Number
1
Dosage Form
-
Strength
2MG/5ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CHILDRENS CETIRIZINE HYDROCHLORIDE ALLERGY
Product Number
2
Dosage Form
-
Strength
5MG/5ML
Approval Date
2008-04-22
Active Ingredient
CETIRIZINE HYDROCHLORIDE
Application Number
90188
Product Number
2
Dosage Form
-
Strength
5MG/5ML
Approval Date
2008-04-22
Regulatory Status
Discontinued
Drug Name
CHILDRENS CETIRIZINE HYDROCHLORIDE HIVES RELIEF
Product Number
1
Dosage Form
-
Strength
5MG/5ML
Approval Date
2008-04-22
Active Ingredient
CETIRIZINE HYDROCHLORIDE
Application Number
90188
Product Number
1
Dosage Form
-
Strength
5MG/5ML
Approval Date
2008-04-22
Regulatory Status
Discontinued
Drug Name
CHLORPHENIRAMINE MALEATE
Product Number
1
Dosage Form
-
Strength
2MG/5ML
Approval Date
1982-02-10
Active Ingredient
CHLORPHENIRAMINE MALEATE
Application Number
87520
Product Number
1
Dosage Form
-
Strength
2MG/5ML
Approval Date
1982-02-10
Regulatory Status
Discontinued
Drug Name
CHLORPROMAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
1999-01-26
Active Ingredient
CHLORPROMAZINE HYDROCHLORIDE
Application Number
40224
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
1999-01-26
Regulatory Status
Discontinued
Drug Name
CHLORPROMAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
30MG/ML
Approval Date
1999-12-30
Active Ingredient
CHLORPROMAZINE HYDROCHLORIDE
Application Number
40231
Product Number
1
Dosage Form
-
Strength
30MG/ML
Approval Date
1999-12-30
Regulatory Status
Discontinued
Drug Name
CIMETIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE/5ML
Approval Date
1997-01-27
Active Ingredient
CIMETIDINE HYDROCHLORIDE
Application Number
74553
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE/5ML
Approval Date
1997-01-27
Regulatory Status
Discontinued
Drug Name
CIMETIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE/5ML
Approval Date
2000-03-15
Active Ingredient
CIMETIDINE HYDROCHLORIDE
Application Number
75560
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE/5ML
Approval Date
2000-03-15
Regulatory Status
Discontinued
Drug Name
CITALOPRAM HYDROBROMIDE
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE/5ML
Approval Date
2005-11-15
Active Ingredient
CITALOPRAM HYDROBROMIDE
Application Number
77601
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE/5ML
Approval Date
2005-11-15
Regulatory Status
Discontinued
Drug Name
CYCLOSPORINE
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
2005-01-05
Active Ingredient
CYCLOSPORINE
Application Number
65167
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
2005-01-05
Regulatory Status
Discontinued
Drug Name
CYPROHEPTADINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
2MG/5ML
Approval Date
2013-03-28
Active Ingredient
CYPROHEPTADINE HYDROCHLORIDE
Application Number
91295
Product Number
1
Dosage Form
-
Strength
2MG/5ML
Approval Date
2013-03-28
Regulatory Status
Discontinued
Drug Name
DOXEPIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE/ML
Approval Date
2004-01-15
Active Ingredient
DOXEPIN HYDROCHLORIDE
Application Number
75924
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE/ML
Approval Date
2004-01-15
Regulatory Status
Discontinued
Drug Name
FLUOXETINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/5ML
Approval Date
2002-01-30
Active Ingredient
FLUOXETINE HYDROCHLORIDE
Application Number
76015
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/5ML
Approval Date
2002-01-30
Regulatory Status
Discontinued
Drug Name
H-CORT
Product Number
1
Dosage Form
-
Strength
0.5%
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE
Application Number
86823
Product Number
1
Dosage Form
-
Strength
0.5%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
H-CORT
Product Number
1
Dosage Form
-
Strength
0.5%
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE
Application Number
86824
Product Number
1
Dosage Form
-
Strength
0.5%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Number
1
Dosage Form
-
Strength
500MG/15ML;7.5MG/15ML
Approval Date
1998-03-13
Active Ingredient
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Application Number
40182
Product Number
1
Dosage Form
-
Strength
500MG/15ML;7.5MG/15ML
Approval Date
1998-03-13
Regulatory Status
Discontinued
Drug Name
LORATADINE
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
2004-10-05
Active Ingredient
LORATADINE
Application Number
75565
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
2004-10-05
Regulatory Status
Discontinued
Drug Name
MIDAZOLAM HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE/ML
Approval Date
2005-09-09
Active Ingredient
MIDAZOLAM HYDROCHLORIDE
Application Number
77115
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE/ML
Approval Date
2005-09-09
Regulatory Status
Discontinued
Drug Name
OXYBUTYNIN CHLORIDE
Product Number
1
Dosage Form
-
Strength
5MG/5ML
Approval Date
1997-10-15
Active Ingredient
OXYBUTYNIN CHLORIDE
Application Number
74997
Product Number
1
Dosage Form
-
Strength
5MG/5ML
Approval Date
1997-10-15
Regulatory Status
Discontinued
Drug Name
OXYBUTYNIN CHLORIDE
Product Number
1
Dosage Form
-
Strength
5MG/5ML
Approval Date
1998-12-18
Active Ingredient
OXYBUTYNIN CHLORIDE
Application Number
75137
Product Number
1
Dosage Form
-
Strength
5MG/5ML
Approval Date
1998-12-18
Regulatory Status
Discontinued
Drug Name
OXYCODONE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
100MG/5ML
Approval Date
2017-08-15
Active Ingredient
OXYCODONE HYDROCHLORIDE
Application Number
206822
Product Number
1
Dosage Form
-
Strength
100MG/5ML
Approval Date
2017-08-15
Regulatory Status
Discontinued
Drug Name
PERPHENAZINE
Product Number
1
Dosage Form
-
Strength
16MG/5ML
Approval Date
2001-05-25
Active Ingredient
PERPHENAZINE
Application Number
40360
Product Number
1
Dosage Form
-
Strength
16MG/5ML
Approval Date
2001-05-25
Regulatory Status
Discontinued
Drug Name
PREDNISOLONE
Product Number
1
Dosage Form
-
Strength
15MG/5ML
Approval Date
2003-03-05
Active Ingredient
PREDNISOLONE
Application Number
40399
Product Number
1
Dosage Form
-
Strength
15MG/5ML
Approval Date
2003-03-05
Regulatory Status
Discontinued
Drug Name
PREDNISOLONE
Product Number
1
Dosage Form
-
Strength
5MG/5ML
Approval Date
2005-08-25
Active Ingredient
PREDNISOLONE
Application Number
40570
Product Number
1
Dosage Form
-
Strength
5MG/5ML
Approval Date
2005-08-25
Regulatory Status
Discontinued
Drug Name
PREDNISOLONE SODIUM PHOSPHATE
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/5ML
Approval Date
2002-12-23
Active Ingredient
PREDNISOLONE SODIUM PHOSPHATE
Application Number
76123
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/5ML
Approval Date
2002-12-23
Regulatory Status
Discontinued
Drug Name
PREDNISOLONE SODIUM PHOSPHATE
Product Number
1
Dosage Form
-
Strength
EQ 30MG BASE/5ML
Approval Date
2020-03-11
Active Ingredient
PREDNISOLONE SODIUM PHOSPHATE
Application Number
204962
Product Number
1
Dosage Form
-
Strength
EQ 30MG BASE/5ML
Approval Date
2020-03-11
Regulatory Status
Discontinued
Drug Name
PROMETHAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
6.25MG/5ML
Approval Date
1982-01-01
Active Ingredient
PROMETHAZINE HYDROCHLORIDE
Application Number
87518
Product Number
1
Dosage Form
-
Strength
6.25MG/5ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PROMETHAZINE HYDROCHLORIDE AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
10MG/5ML;6.25MG/5ML
Approval Date
1988-12-22
Active Ingredient
CODEINE PHOSPHATE; PROMETHAZINE HYDROCHLORIDE
Application Number
89647
Product Number
1
Dosage Form
-
Strength
10MG/5ML;6.25MG/5ML
Approval Date
1988-12-22
Regulatory Status
Discontinued
Drug Name
PROMETHAZINE WITH CODEINE
Product Number
1
Dosage Form
-
Strength
10MG/5ML;6.25MG/5ML
Approval Date
2006-01-31
Active Ingredient
CODEINE PHOSPHATE; PROMETHAZINE HYDROCHLORIDE
Application Number
40650
Product Number
1
Dosage Form
-
Strength
10MG/5ML;6.25MG/5ML
Approval Date
2006-01-31
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 15MG BASE/ML
Approval Date
2007-09-21
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
77405
Product Number
1
Dosage Form
-
Strength
EQ 15MG BASE/ML
Approval Date
2007-09-21
Regulatory Status
Discontinued
Drug Name
RISPERIDONE
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
2009-07-29
Active Ingredient
RISPERIDONE
Application Number
77719
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
2009-07-29
Regulatory Status
Discontinued
Drug Name
SULFATRIM
Product Number
2
Dosage Form
-
Strength
200MG/5ML;40MG/5ML
Approval Date
1983-01-07
Active Ingredient
SULFAMETHOXAZOLE; TRIMETHOPRIM
Application Number
18615
Product Number
2
Dosage Form
-
Strength
200MG/5ML;40MG/5ML
Approval Date
1983-01-07
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE
Product Number
1
Dosage Form
-
Strength
80MG/15ML
Approval Date
1982-01-01
Active Ingredient
THEOPHYLLINE
Application Number
86720
Product Number
1
Dosage Form
-
Strength
80MG/15ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
30MG/ML
Approval Date
1997-08-28
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
40187
Product Number
1
Dosage Form
-
Strength
30MG/ML
Approval Date
1997-08-28
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
1998-05-29
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
40213
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
1998-05-29
Regulatory Status
Discontinued
Drug Name
TRIPROLIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
1.25MG/5ML
Approval Date
1982-02-10
Active Ingredient
TRIPROLIDINE HYDROCHLORIDE
Application Number
87514
Product Number
1
Dosage Form
-
Strength
1.25MG/5ML
Approval Date
1982-02-10
Regulatory Status
Discontinued
Related Databases
-
FDA Inspections
0 View
-
EDQM CEP
0 View
-
KDMF
0 View
-
Japan DMF
0 View
-
Eudra GMP
0 View
-
NDC Database
0 View
-
FDA Approved Drugs Database
68 View
-
Drug Prices in Switzerland
0 View
Drug Status Breakdown
36 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
BROMPHENIRAMINE MALEATE
Application Number
87517
Product Number
1
Active Ingredient
BROMPHENIRAMINE MALEATE
Dosage Form
-
Strength
2MG/5ML
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.