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Olanzapine

NDC 67046-0072 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202862
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOLANZAPINE (20 mg/1)
Marketing started20260619
Package count1

External sources

Source: openFDA. Public-domain (CC0).