FDA Drug Application (202917) for METFORMIN HYDROCHLORIDE by SUN PHARMA GLOBAL

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Application Number202917
Product Number001
FormTABLET, EXTENDED RELEASE;ORAL
Dosage500MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB3 Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameMETFORMIN HYDROCHLORIDE
Active IngredientMETFORMIN HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient METFORMIN HYDROCHLORIDE32


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