Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 002918
Company: POYTHRESS
Company: POYTHRESS
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| BENSULFOID | SULFUR | 33.32% | POWDER;TOPICAL | Discontinued | None | No | No |