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Phentermine Hydrochloride

NDC 43547-404 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSolco Healthcare U.S., LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040377
Dosage form / routeTABLET · ORAL
Active ingredientsPHENTERMINE HYDROCHLORIDE (37.5 mg/1)
Marketing started20020104
Package count4

External sources

Source: openFDA. Public-domain (CC0).