NDC 69452-433

divalproex sodium 125 mg tablet, delayed release

On the label: Bionpharma Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
OrBion Pharmaceuticals Private LimitedKancheepuram, IndiaMakes it, tests it, packages it and labels it No problems foundOct 27, 2025 · 6 inspections

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Valproic Acid: every company that makes it
Form
tablet, delayed release, oral
Strength
125 mg
Approval
ANDA ANDA078853
On the market since
Jun 26, 2024
Package NDCs
69452-433-13 69452-433-20 69452-433-30
Official label
DailyMed (National Library of Medicine), updated Apr 30, 2026

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