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Phentermine Hydrochloride

NDC 43063-596 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040526
Dosage form / routeTABLET · ORAL
Active ingredientsPHENTERMINE HYDROCHLORIDE (30 mg/1)
Marketing started20130812
Package count13

External sources

Source: openFDA. Public-domain (CC0).