NDC 77771-177

Gabapentin 600 mg tablet

On the label: Radha Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it and tests it Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Gabapentin: every company that makes it
Form
tablet, oral
Strength
600 mg
Approval
ANDA ANDA205101
On the market since
Nov 3, 2023
Package NDCs
77771-177-05 77771-177-90
Official label
DailyMed (National Library of Medicine), updated Mar 11, 2026

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