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Acebutolol Hydrochloride

NDC 65162-669 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075047
Dosage form / routeCAPSULE · ORAL
Active ingredientsACEBUTOLOL HYDROCHLORIDE (200 mg/1)
Marketing started20091201
Package count2

External sources

Source: openFDA. Public-domain (CC0).