| NDC Code | 42806-081-05 |
|---|
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (42806-081-05) |
|---|
| Product NDC | 42806-081 |
|---|
| 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 | Epic Pharma, 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 |
|---|