FDA NDC Directory · JSON-LD · Markdown

Olanzapine

NDC 71335-2599 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA090798
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOLANZAPINE (5 mg/1)
Marketing started20120423
Package count5

External sources

Source: openFDA. Public-domain (CC0).