NDC 0440-5563

Gabapentin 800 mg tablet, film coated

On the label: Liberty Pharmaceuticals, Inc.. It's a repackaged product: Liberty Pharmaceuticals, Inc. rebottles it from Exelan Pharmaceuticals, Inc.'s NDC 76282-406.

Where the pills inside were made

Central Islip, NY, United States · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Aug 9, 2024. 9 inspections on record.

Hauppauge, NY, United States · makes it and tests it

No problems found Last FDA inspection Oct 25, 2023. 18 inspections on record.

Central Islip, NY, United States · makes it, tests it and packages it

Problems found, fixed voluntarily Last FDA inspection Jul 17, 2026. 4 inspections on record.

May 14, 2020 · Class III · Terminated
Failed Impurities/Degradation Specifications; failure of Impurity A test at the 12-month long-term stability testing.
Lots: Lot # NB900413, Exp. 12/2020

Generic drug: Gabapentin: see every company that makes it
Form: tablet, film coated
Strength: 800 mg
Approval: ANDA ANDA202764
On the market since: Nov 2, 2012
Package NDCs: 0440-5563-05 0440-5563-30 0440-5563-60 0440-5563-81 0440-5563-90 0440-5563-91 0440-5563-92 0440-5563-94
Official label: DailyMed (National Library of Medicine), updated Aug 9, 2016

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