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Divalproex sodium

NDC 55154-3552 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerCardinal Health 107, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078979
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDIVALPROEX SODIUM (125 mg/1)
Marketing started20090123
Package count1

External sources

Source: openFDA. Public-domain (CC0).