NDC 71335-0254 – Gabapentin
Gabapentin 800 mg/1 · Tablet · Oral
Product NDC71335-0254
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077662
- Marketed since
- April 1, 2006
- Listing expires
- December 31, 2026
Active ingredients
- Gabapentin 800 mg/1
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0254-1 | 30 TABLET in 1 BOTTLE (71335-0254-1) | Jul 19, 2018 |
| 71335-0254-2 | 60 TABLET in 1 BOTTLE (71335-0254-2) | May 4, 2018 |
| 71335-0254-3 | 90 TABLET in 1 BOTTLE (71335-0254-3) | Mar 15, 2018 |
| 71335-0254-4 | 180 TABLET in 1 BOTTLE (71335-0254-4) | May 11, 2018 |
| 71335-0254-5 | 120 TABLET in 1 BOTTLE (71335-0254-5) | Apr 17, 2018 |
| 71335-0254-6 | 100 TABLET in 1 BOTTLE (71335-0254-6) | Oct 8, 2024 |
| 71335-0254-7 | 84 TABLET in 1 BOTTLE (71335-0254-7) | Apr 3, 2018 |
| 71335-0254-8 | 112 TABLET in 1 BOTTLE (71335-0254-8) | Oct 8, 2024 |
| 71335-0254-9 | 135 TABLET in 1 BOTTLE (71335-0254-9) | Oct 8, 2024 |
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