FDA NDC Directory · JSON-LD · Markdown

Olanzapine

NDC 42658-159 · HUMAN PRESCRIPTION DRUG · TABLET, ORALLY DISINTEGRATING

Labeler / ManufacturerHisun Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206892
Dosage form / routeTABLET, ORALLY DISINTEGRATING · ORAL
Active ingredientsOLANZAPINE (20 mg/20mg)
Marketing started20250101
Package count3

External sources

Source: openFDA. Public-domain (CC0).