FDA NDC Directory · JSON-LD · Markdown

OLANZAPINE

NDC 72303-0840 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameOlanzapine
Labeler / ManufacturerHEC Pharm USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206238
Dosage form / routeTABLET · ORAL
Active ingredientsOLANZAPINE (20 mg/1)
Marketing started20181130
Package count1

External sources

Source: openFDA. Public-domain (CC0).