| NDC Code | 0574-0116-01 |
|---|
| Package Description | 100 TABLET, COATED in 1 BOTTLE (0574-0116-01) |
|---|
| Product NDC | 0574-0116 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Benzphetamine Hydrochloride |
|---|
| Non-Proprietary Name | Benzphetamine Hydrochloride |
|---|
| Dosage Form | TABLET, COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20070501 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040578 |
|---|
| Manufacturer | Paddock Laboratories, Inc. |
|---|
| 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 |
|---|