FDA NDC Directory · JSON-LD · Markdown

Temozolomide

NDC 70301-2011 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameTEMOZOLOMIDE
Labeler / ManufacturerOPKO Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203898
Dosage form / routeCAPSULE · ORAL
Active ingredientsTEMOZOLOMIDE (250 mg/1)
Marketing started20260916
Package count1

External sources

Source: openFDA. Public-domain (CC0).