FDA Drug Application (078919) for DIVALPROEX SODIUM by ZYDUS PHARMS USA INC

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Application Number078919
Product Number001
FormCAPSULE, DELAYED REL PELLETS;ORAL
DosageEQ 125MG VALPROIC ACID
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameDIVALPROEX SODIUM
Active IngredientDIVALPROEX SODIUM

Active IngredientCount
List of drugs with Active Ingredient DIVALPROEX SODIUM4


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