NDC 71610-630 – Gabapentin
Gabapentin 800 mg/1 · Tablet · Oral
Product NDC71610-630
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA214957
- Marketed since
- October 1, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Gabapentin 800 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71610-630-30 | 30 TABLET in 1 BOTTLE (71610-630-30) | Apr 20, 2022 |
| 71610-630-45 | 45 TABLET in 1 BOTTLE (71610-630-45) | Apr 20, 2022 |
| 71610-630-53 | 60 TABLET in 1 BOTTLE (71610-630-53) | Apr 20, 2022 |
| 71610-630-60 | 90 TABLET in 1 BOTTLE (71610-630-60) | Apr 20, 2022 |
| 71610-630-70 | 120 TABLET in 1 BOTTLE (71610-630-70) | Apr 20, 2022 |
| 71610-630-73 | 135 TABLET in 1 BOTTLE (71610-630-73) | Apr 20, 2022 |
| 71610-630-80 | 180 TABLET in 1 BOTTLE (71610-630-80) | Jan 25, 2022 |
| 71610-630-92 | 270 TABLET in 1 BOTTLE (71610-630-92) | Jan 25, 2022 |
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