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

Active IngredientCount
List of drugs with Active Ingredient DIVALPROEX SODIUM4


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