FDA NDC Directory · JSON-LD · Markdown

Olanzapine

NDC 33342-067 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202862
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOLANZAPINE (2.5 mg/1)
Marketing started20140822
Package count4

External sources

Source: openFDA. Public-domain (CC0).