| NDC Code | 68382-703-10 |
|---|
| Package Description | 1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68382-703-10) |
|---|
| Product NDC | 68382-703 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Phentermine Hydrochloride |
|---|
| Non-Proprietary Name | Phentermine Hydrochloride |
|---|
| Dosage Form | TABLET, ORALLY DISINTEGRATING |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180208 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA204663 |
|---|
| Manufacturer | Zydus Pharmaceuticals USA Inc. |
|---|
| Substance Name | PHENTERMINE HYDROCHLORIDE |
|---|
| Strength | 15 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC] |
|---|
| DEA Schedule | CIV |
|---|