NDC Code | 54569-5912-1 |
Package Description | 60 TABLET in 1 BOTTLE (54569-5912-1) |
Product NDC | 54569-5912 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Benzphetamine Hydrochloride |
Non-Proprietary Name | Benzphetamine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20100721 |
Marketing Category Name | ANDA |
Application Number | ANDA090968 |
Manufacturer | A-S Medication Solutions LLC |
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 |