FDA NDC Directory · JSON-LD · Markdown

Temozolomide

NDC 47335-930 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA201742
Dosage form / routeCAPSULE · ORAL
Active ingredientsTEMOZOLOMIDE (180 mg/1)
Marketing started20140213
Package count6

External sources

Source: openFDA. Public-domain (CC0).