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Phentermine hydrochloride

NDC 11534-159 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic namephentermine hydrochloride
Labeler / ManufacturerSUNRISE PHARMACEUTICAL, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA205017
Dosage form / routeCAPSULE · ORAL
Active ingredientsPHENTERMINE HYDROCHLORIDE (37.5 mg/1)
Marketing started20170124
Package count3

External sources

Source: openFDA. Public-domain (CC0).