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Lomustine

NDC 52536-341 · HUMAN PRESCRIPTION DRUG · CAPSULE, GELATIN COATED

Generic namelomustine
Labeler / ManufacturerWilshire Pharmaceuticals, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA017588
Dosage form / routeCAPSULE, GELATIN COATED · ORAL
Active ingredientsLOMUSTINE (40 mg/1)
Marketing started20260415
Package count1

External sources

Source: openFDA. Public-domain (CC0).