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

Active IngredientCount
List of drugs with Active Ingredient DIVALPROEX SODIUM4


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