ScieGen Pharmaceuticals, INC.
Hauppauge, NY, United States · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection May 15, 2026. 15 inspections on record, 1 with serious problems.
NDC 77771-178
Gabapentin 800 mg tablet
On the label: Radha Pharmaceuticals, Inc..
Where it's made
Product details
- Generic drug
- Gabapentin: see every company that makes it
- Form
- tablet, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA205101
- On the market since
- Nov 3, 2023
- Package NDCs
77771-178-0577771-178-90- Official label
- DailyMed (National Library of Medicine), updated Mar 11, 2026
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