FDA NDC Directory · JSON-LD · Markdown
NDC 51672-1371 · HUMAN PRESCRIPTION DRUG · SPRAY
| Labeler / Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA208842 |
| Dosage form / route | SPRAY · TOPICAL |
| Active ingredients | CLOBETASOL PROPIONATE (.05 g/mL) |
| Marketing started | 20180326 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).