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Erlotinib

NDC 72485-218 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameErlotinib hydrochloride
Labeler / ManufacturerArmas Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211960
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsERLOTINIB HYDROCHLORIDE (100 mg/1)
Marketing started20191106
Package count1

External sources

Source: openFDA. Public-domain (CC0).