NDC 63629-4698

Divalproex sodium 500 mg tablet, film coated, extended release

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Aurobindo Pharma Limited's NDC 65862-595.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMahabubnagar, IndiaMakes it and tests it Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Valproic Acid: every company that makes it
Form
tablet, film coated, extended release, oral
Strength
500 mg
Approval
ANDA ANDA202419
On the market since
Jun 2, 2014
Package NDCs
63629-4698-1 63629-4698-2 63629-4698-3 63629-4698-4
Official label
DailyMed (National Library of Medicine), updated Aug 19, 2025

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