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Phentermine Hydrochloride

NDC 68094-702 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPrecision Dose Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA200272
Dosage form / routeTABLET · ORAL
Active ingredientsPHENTERMINE HYDROCHLORIDE (37.5 mg/1)
Marketing started20240215
Marketing ended20280430
Package count2

External sources

Source: openFDA. Public-domain (CC0).