| NDC Code | 43063-532-30 |
|---|
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-532-30) |
|---|
| Product NDC | 43063-532 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Diethylpropion Hydrochloride |
|---|
| Proprietary Name Suffix | Er |
|---|
| Non-Proprietary Name | Diethylpropion Hydrochloride |
|---|
| Dosage Form | TABLET, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20111024 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA091680 |
|---|
| 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 |
|---|