| NDC Code | 71335-0507-2 |
|---|
| Package Description | 7 TABLET, FILM COATED in 1 BOTTLE (71335-0507-2) |
|---|
| 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 |
|---|