FDA Drug Application (078791) for DIVALPROEX SODIUM by IMPAX LABS

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Application Number078791
Product Number001
FormTABLET, EXTENDED RELEASE;ORAL
DosageEQ 250MG VALPROIC ACID
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameDIVALPROEX SODIUM
Active IngredientDIVALPROEX SODIUM



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