FDA NDC Directory · JSON-LD · Markdown
NDC 51672-2151 · HUMAN OTC DRUG · SOLUTION
| Generic name | Minoxidil Solution |
|---|---|
| Labeler / Manufacturer | Sun Pharmaceutical Industries, Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA217998 |
| Dosage form / route | SOLUTION · TOPICAL |
| Active ingredients | MINOXIDIL (50 mg/mL) |
| Marketing started | 20250801 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).