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Olanzapine

NDC 87441-062 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerUnit Dose Solutions, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076255
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOLANZAPINE (5 mg/1)
Marketing started20260629
Package count1

External sources

Source: openFDA. Public-domain (CC0).