| NDC Code | 24090-722-85 |
|---|
| Package Description | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (24090-722-85) |
|---|
| Product NDC | 24090-722 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Suprenza |
|---|
| Non-Proprietary Name | Phentermine Hydrochloride |
|---|
| Dosage Form | TABLET, ORALLY DISINTEGRATING |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20121214 |
|---|
| End Marketing Date | 20180930 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA202088 |
|---|
| Manufacturer | Akrimax Pharmaceuticals, LLC |
|---|
| 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 |
|---|