NDC 63739-995

Divalproex sodium 125 mg capsule

On the label: McKesson Packaging Services Business Unit of McKesson Corporation. It's repackaged: McKesson Packaging Services Business Unit of McKesson Corporation rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-532.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Dr. Reddy's Laboratories LimitedMedchal-Malkajgiri, IndiaMakes it and tests it Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections

Repackaging site

Product details

Generic drug
Valproic Acid: every company that makes it
Form
capsule
Strength
125 mg
Approval
ANDA ANDA078979
On the market since
Jan 23, 2009
Package NDCs
63739-995-10
Official label
DailyMed (National Library of Medicine), updated Dec 20, 2024

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