NDC 0615-8377

Divalproex sodium 500 mg tablet, extended release

On the label: NCS HealthCare of KY, Inc dba Vangard Labs. It's repackaged: NCS HealthCare of KY, Inc dba Vangard Labs rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-261.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Lupin LimitedNagpur, IndiaMakes it and packages it Problems found, fixed voluntarilyJul 11, 2023 · 4 inspections

Repackaging site

Product details

Generic drug
Valproic Acid: every company that makes it
Form
tablet, extended release
Strength
500 mg
Approval
ANDA ANDA209286
On the market since
Sep 18, 2020
Package NDCs
0615-8377-30 0615-8377-39
Official label
DailyMed (National Library of Medicine), updated Sep 13, 2024

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