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Olanzapine

NDC 42658-152 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerHisun Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206924
Dosage form / routeTABLET · ORAL
Active ingredientsOLANZAPINE (7.5 mg/7.5mg)
Marketing started20250101
Package count3

External sources

Source: openFDA. Public-domain (CC0).