NDC 71610-249

Divalproex sodium 500 mg tablet, film coated, extended release

On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged: Aphena Pharma Solutions - Tennessee, Inc. rebottles it from Northstar Rx LLC.'s NDC 16714-485.

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
71610-249-30 71610-249-53 71610-249-60 71610-249-70 71610-249-74 71610-249-80
Official label
DailyMed (National Library of Medicine), updated Jun 15, 2026

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