NDC 68382-106

divalproex sodium 125 mg capsule, coated pellets

On the label: Zydus Pharmaceuticals (USA) Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action

Product details

Generic drug
Valproic Acid: every company that makes it
Form
capsule, coated pellets, oral
Strength
125 mg
Approval
ANDA ANDA078919
On the market since
Jan 27, 2009
Package NDCs
68382-106-01 68382-106-10 68382-106-30 68382-106-77
Official label
DailyMed (National Library of Medicine), updated Apr 6, 2026

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