FDA NDC Directory · JSON-LD · Markdown
NDC 51672-1367 · HUMAN PRESCRIPTION DRUG · GEL
| Labeler / Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA206575 |
| Dosage form / route | GEL · TOPICAL |
| Active ingredients | BENZOYL PEROXIDE (25 mg/g) CLINDAMYCIN PHOSPHATE (10 mg/g) |
| Marketing started | 20190819 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).