FDA NDC Directory · JSON-LD · Markdown

Ojjaara

NDC 81864-101 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameMomelotinib
Labeler / ManufacturerGlaxoSmithKline LLC
Marketing categoryNew Drug Application (innovator) · App NDA216873
Dosage form / routeTABLET · ORAL
Active ingredientsMOMELOTINIB DIHYDROCHLORIDE MONOHYDRATE (200 mg/1)
Marketing started20230915
Package count1

External sources

Source: openFDA. Public-domain (CC0).