NDC Code | 71335-0507-7 |
Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0507-7) |
Product NDC | 71335-0507 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Benzphetamine Hydrochloride |
Non-Proprietary Name | Benzphetamine Hydrochloride |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20151216 |
Marketing Category Name | ANDA |
Application Number | ANDA090346 |
Manufacturer | Bryant Ranch Prepack |
Substance Name | BENZPHETAMINE HYDROCHLORIDE |
Strength | 50 |
Strength Unit | mg/1 |
Pharmacy Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |
DEA Schedule | CIII |