FDA NDC Directory · JSON-LD · Markdown
NDC 51672-2070 · HUMAN OTC DRUG · CREAM
| Labeler / Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA076773 |
| Dosage form / route | CREAM · VAGINAL |
| Active ingredients | MICONAZOLE NITRATE (40 mg/g) |
| Marketing started | 20050302 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).