Capmatinib
Tablet, Film Coated
No FDA structured label text is available for Capmatinib. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Capmatinib Hydrochloride in 2 products
Capmatinib NDC products (2)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 66828-0275 | Capmatinib Hydrochloride 200 mg/1 Tablet, Film Coated | Novartis Pharma Produktions GmbH | DRUG FOR FURTHER PROCESSING |
| 66828-0317 | Capmatinib Hydrochloride 150 mg/1 Tablet, Film Coated | Novartis Pharma Produktions GmbH | DRUG FOR FURTHER PROCESSING |
Frequently asked questions
Who makes Capmatinib?
Capmatinib is listed by 1 labeler in the FDA NDC directory, including Novartis Pharma Produktions GmbH.