FDA NDC Directory · JSON-LD · Markdown
NDC 0078-0709 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Generic name | capmatinib |
|---|---|
| Labeler / Manufacturer | Novartis Pharmaceuticals Corporation |
| Marketing category | New Drug Application (innovator) · App NDA213591 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | CAPMATINIB HYDROCHLORIDE (150 mg/1) |
| Marketing started | 20200506 |
| Package count | 2 |
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