NDC 68071-3472

Gabapentin 800 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-167.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Ascent Pharmaceuticals IncCentral Islip, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections

Repackaging site

Product details

Generic drug
Gabapentin: every company that makes it
Form
tablet
Strength
800 mg
Approval
ANDA ANDA214957
On the market since
Oct 1, 2021
Package NDCs
68071-3472-9
Official label
DailyMed (National Library of Medicine), updated Jul 26, 2023

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