asciminib
Tablet, Film Coated
No FDA structured label text is available for asciminib. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Asciminib Hydrochloride in 3 products
asciminib NDC products (3)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 17088-0156 | Asciminib Hydrochloride 20 mg/1 Tablet, Film Coated | Novartis Pharma Stein AG | DRUG FOR FURTHER PROCESSING |
| 17088-0163 | Asciminib Hydrochloride 40 mg/1 Tablet, Film Coated | Novartis Pharma Stein AG | DRUG FOR FURTHER PROCESSING |
| 17088-0330 | Asciminib Hydrochloride 100 mg/1 Tablet, Film Coated | Novartis Pharma Stein AG | DRUG FOR FURTHER PROCESSING |
Frequently asked questions
Who makes asciminib?
asciminib is listed by 1 labeler in the FDA NDC directory, including Novartis Pharma Stein AG.