NDC 76420-235
Gabapentin 600 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-177.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it
Recalls
- Feb 17, 2023 · Class III · Sciegen Pharmaceuticals Inc
Presence of Foreign Tablets/Capsules: Pharmacist reported presence of some Gabapentin tablets 800 mg comingled in Gabapentin 600 mg 500 count bottles.
Lots: Lot # G177092, Exp. 11/24
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Gabapentin: every company that makes it
- Form
- tablet, oral
- Strength
- 600 mg
- Approval
- ANDA ANDA205101
- On the market since
- Feb 4, 2016
- Package NDCs
76420-235-1276420-235-2476420-235-3076420-235-6076420-235-90- Official label
- DailyMed (National Library of Medicine), updated Jul 7, 2022
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