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



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