| NDC Code | 55289-701-32 |
|---|
| Package Description | 32 TABLET in 1 BOTTLE, PLASTIC (55289-701-32) |
|---|
| Product NDC | 55289-701 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Phentermine Hydrochloride |
|---|
| Non-Proprietary Name | Phentermine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20120815 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040876 |
|---|
| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
|---|
| Substance Name | PHENTERMINE HYDROCHLORIDE |
|---|
| Strength | 37.5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC] |
|---|
| DEA Schedule | CIV |
|---|