| NDC Code | 55289-368-07 |
|---|
| Package Description | 7 TABLET in 1 BOTTLE, PLASTIC (55289-368-07) |
|---|
| Product NDC | 55289-368 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Diethylpropion Hydrochloride Controlled-release |
|---|
| Non-Proprietary Name | Diethylpropion Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19601117 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA012546 |
|---|
| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
|---|
| Substance Name | DIETHYLPROPION HYDROCHLORIDE |
|---|
| Strength | 75 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |
|---|
| DEA Schedule | CIV |
|---|