NDC 68382-205

Gabapentin 800 mg tablet, film coated

On the label: Zydus Pharmaceuticals (USA) Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action

Product details

Generic drug
Gabapentin: every company that makes it
Form
tablet, film coated, oral
Strength
800 mg
Approval
ANDA ANDA078926
On the market since
Oct 16, 2012
Package NDCs
68382-205-01 68382-205-05 68382-205-10 68382-205-30 68382-205-77
Official label
DailyMed (National Library of Medicine), updated Sep 8, 2025

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