FDA NDC Directory · JSON-LD · Markdown
NDC 0472-1738 · HUMAN PRESCRIPTION DRUG · SUPPOSITORY
| Labeler / Manufacturer | Actavis Pharma, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA073508 |
| Dosage form / route | SUPPOSITORY · VAGINAL |
| Active ingredients | MICONAZOLE NITRATE (200 mg/1) |
| Marketing started | 19950118 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).