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Phentermine hydrochloride

NDC 71205-668 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namephentermine hydrochloride
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA205008
Dosage form / routeTABLET · ORAL
Active ingredientsPHENTERMINE HYDROCHLORIDE (37.5 mg/1)
Marketing started20170124
Package count4

External sources

Source: openFDA. Public-domain (CC0).