FDA Drug Application (203068) for PHENTERMINE HYDROCHLORIDE by AUROLIFE PHARMA LLC

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Application Number203068
Product Number001
FormTABLET;ORAL
Dosage37.5MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AA Products in conventional dosage forms not presenting bioequivalence problems
Reference Drug
Drug NamePHENTERMINE HYDROCHLORIDE
Active IngredientPHENTERMINE HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient PHENTERMINE HYDROCHLORIDE11


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