FDA NDC Directory · JSON-LD · Markdown
NDC 60290-002 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | Umedica Laboratories USA Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA209302 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | SILDENAFIL CITRATE (50 mg/1) |
| Marketing started | 20260215 |
| Package count | 4 |
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