FDA NDC Directory · JSON-LD · Markdown

Guanfacine

NDC 24658-730 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPuraCap Laboratories LLC dba Blu Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA074673
Dosage form / routeTABLET · ORAL
Active ingredientsGUANFACINE HYDROCHLORIDE (1 mg/1)
Marketing started20161114
Package count1

External sources

Source: openFDA. Public-domain (CC0).