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Guanfacine

NDC 29300-463 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerUnichem Pharmaceuticals (USA), Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA219033
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGUANFACINE HYDROCHLORIDE (4 mg/1)
Marketing started20241119
Package count1

External sources

Source: openFDA. Public-domain (CC0).