FDA Drug Application (077615) for DIVALPROEX SODIUM by NU PHARM

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Application Number077615
Product Number001
FormTABLET, DELAYED RELEASE;ORAL
DosageEQ 500MG 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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