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Phenoxybenzamine hydrochloride

NDC 60219-1502 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212568
Dosage form / routeCAPSULE · ORAL
Active ingredientsPHENOXYBENZAMINE HYDROCHLORIDE (10 mg/1)
Marketing started20201030
Package count1

External sources

Source: openFDA. Public-domain (CC0).