| NDC Code | 52605-022-01 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (52605-022-01) |
|---|
| Product NDC | 52605-022 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Phentermine Hydrochloride |
|---|
| Non-Proprietary Name | Phentermine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20161118 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA206342 |
|---|
| Manufacturer | POLYGEN 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 |
|---|