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Guanfacine Hydrochloride

NDC 72603-268 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNORTHSTAR RX LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218326
Dosage form / routeTABLET · ORAL
Active ingredientsGUANFACINE HYDROCHLORIDE (1 mg/1)
Marketing started20240715
Package count1

External sources

Source: openFDA. Public-domain (CC0).