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GUANFACINE

NDC 62332-747 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217269
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGUANFACINE HYDROCHLORIDE (3 mg/1)
Marketing started20230808
Package count2

External sources

Source: openFDA. Public-domain (CC0).