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Letrozole

NDC 80005-139 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCarnegie Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091191
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLETROZOLE (2.5 mg/1)
Marketing started20260630
Package count2

External sources

Source: openFDA. Public-domain (CC0).