G&W Laboratories
FDA Approved Drugs
G&W Laboratories
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 15
- Latest Approval Date Jul 05, 2019
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Overview
Company
G&W Laboratories
Country
U.S.A
Website
Social Profiles
Company Snapshot
G&W Laboratories
G&W Laboratories111 Coolidge StreetSouth Plainfield, NJ 07080-3895, USA
U.S.A
www.gwlabs.com/ Quality Assurance & Scientific Affairs: qaqcregulatory@gwlabs.com Sales: salesandmarketing@gwlabs.com Human Resources: HR@gwlabs.com View on MapFDA Approved Drug Records ( 15 records )
Drug Name
AMANTADINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG/5ML
Approval Date
1990-10-30
Active Ingredient
AMANTADINE HYDROCHLORIDE
Application Number
72655
Product Number
1
Dosage Form
-
Strength
50MG/5ML
Approval Date
1990-10-30
Regulatory Status
Discontinued
Drug Name
CAPTOPRIL
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1996-08-30
Active Ingredient
CAPTOPRIL
Application Number
74590
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1996-08-30
Regulatory Status
Discontinued
Drug Name
CAPTOPRIL
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
1996-08-30
Active Ingredient
CAPTOPRIL
Application Number
74590
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
1996-08-30
Regulatory Status
Discontinued
Drug Name
CAPTOPRIL
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
1996-08-30
Active Ingredient
CAPTOPRIL
Application Number
74590
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
1996-08-30
Regulatory Status
Discontinued
Drug Name
CAPTOPRIL
Product Number
4
Dosage Form
-
Strength
12.5MG
Approval Date
1996-08-30
Active Ingredient
CAPTOPRIL
Application Number
74590
Product Number
4
Dosage Form
-
Strength
12.5MG
Approval Date
1996-08-30
Regulatory Status
Discontinued
Drug Name
CIMETIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE/5ML
Approval Date
1994-06-01
Active Ingredient
CIMETIDINE HYDROCHLORIDE
Application Number
74176
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE/5ML
Approval Date
1994-06-01
Regulatory Status
Discontinued
Drug Name
CLINDAMYCIN PHOSPHATE
Product Number
1
Dosage Form
-
Strength
EQ 1% BASE
Approval Date
1988-09-01
Active Ingredient
CLINDAMYCIN PHOSPHATE
Application Number
62811
Product Number
1
Dosage Form
-
Strength
EQ 1% BASE
Approval Date
1988-09-01
Regulatory Status
Discontinued
Drug Name
FLUOXETINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 60MG BASE
Approval Date
2019-07-05
Active Ingredient
FLUOXETINE HYDROCHLORIDE
Application Number
212191
Product Number
1
Dosage Form
-
Strength
EQ 60MG BASE
Approval Date
2019-07-05
Regulatory Status
Discontinued
Drug Name
HYDROCORTISONE
Product Number
1
Dosage Form
-
Strength
1%
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE
Application Number
84059
Product Number
1
Dosage Form
-
Strength
1%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MESALAMINE
Product Number
1
Dosage Form
-
Strength
4GM/60ML
Approval Date
2004-09-30
Active Ingredient
MESALAMINE
Application Number
76841
Product Number
1
Dosage Form
-
Strength
4GM/60ML
Approval Date
2004-09-30
Regulatory Status
Discontinued
Drug Name
METAPROTERENOL SULFATE
Product Number
1
Dosage Form
-
Strength
10MG/5ML
Approval Date
1991-08-30
Active Ingredient
METAPROTERENOL SULFATE
Application Number
73034
Product Number
1
Dosage Form
-
Strength
10MG/5ML
Approval Date
1991-08-30
Regulatory Status
Discontinued
Drug Name
NYSTATIN
Product Number
1
Dosage Form
-
Strength
100,000 UNITS/ML
Approval Date
1982-07-14
Active Ingredient
NYSTATIN
Application Number
62349
Product Number
1
Dosage Form
-
Strength
100,000 UNITS/ML
Approval Date
1982-07-14
Regulatory Status
Discontinued
Drug Name
PROMETH VC PLAIN
Product Number
1
Dosage Form
-
Strength
5MG/5ML;6.25MG/5ML
Approval Date
1984-11-08
Active Ingredient
PHENYLEPHRINE HYDROCHLORIDE; PROMETHAZINE HYDROCHLORIDE
Application Number
88761
Product Number
1
Dosage Form
-
Strength
5MG/5ML;6.25MG/5ML
Approval Date
1984-11-08
Regulatory Status
Discontinued
Drug Name
PROMETH W/ DEXTROMETHORPHAN
Product Number
1
Dosage Form
-
Strength
15MG/5ML;6.25MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-10-31
Active Ingredient
DEXTROMETHORPHAN HYDROBROMIDE; PROMETHAZINE HYDROCHLORIDE
Application Number
88762
Product Number
1
Dosage Form
-
Strength
15MG/5ML;6.25MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-10-31
Regulatory Status
Discontinued
Drug Name
SELEGILINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1996-08-02
Active Ingredient
SELEGILINE HYDROCHLORIDE
Application Number
74537
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1996-08-02
Regulatory Status
Discontinued
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Drug Status Breakdown
15 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
AMANTADINE HYDROCHLORIDE
Application Number
72655
Product Number
1
Active Ingredient
AMANTADINE HYDROCHLORIDE
Dosage Form
-
Strength
50MG/5ML
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