NDC 61919-104
Gabapentin 800 mg tablet, film coated
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-205.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it and relabels it
Product details
- Generic drug
- Gabapentin: every company that makes it
- Form
- tablet, film coated
- Strength
- 800 mg
- Approval
- ANDA ANDA078926
- On the market since
- Jan 1, 2014
- Package NDCs
61919-104-3061919-104-6061919-104-90- Official label
- DailyMed (National Library of Medicine), updated Nov 4, 2015
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?