Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 075678
Company: ACTAVIS ELIZABETH
Company: ACTAVIS ELIZABETH
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| PEMOLINE | PEMOLINE | 37.5MG | TABLET, CHEWABLE;ORAL | Discontinued | None | No | No |