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Divalproex sodium

NDC 46708-821 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA218793
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDIVALPROEX SODIUM (125 mg/1)
Marketing started20241223
Package count3

External sources

Source: openFDA. Public-domain (CC0).