NDC 71335-2037 – Gabapentin
Gabapentin 800 mg/1 · Tablet · Oral
Product NDC71335-2037
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA206402
- Marketed since
- November 1, 2015
- Listing expires
- December 31, 2027
Active ingredients
- Gabapentin 800 mg/1
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2037-1 | 30 TABLET in 1 BOTTLE (71335-2037-1) | Apr 13, 2022 |
| 71335-2037-2 | 60 TABLET in 1 BOTTLE (71335-2037-2) | Mar 7, 2022 |
| 71335-2037-3 | 90 TABLET in 1 BOTTLE (71335-2037-3) | Mar 7, 2022 |
| 71335-2037-4 | 180 TABLET in 1 BOTTLE (71335-2037-4) | Jan 30, 2025 |
| 71335-2037-5 | 120 TABLET in 1 BOTTLE (71335-2037-5) | Mar 14, 2022 |
| 71335-2037-6 | 100 TABLET in 1 BOTTLE (71335-2037-6) | Jan 30, 2025 |
| 71335-2037-7 | 84 TABLET in 1 BOTTLE (71335-2037-7) | Jan 30, 2025 |
| 71335-2037-8 | 112 TABLET in 1 BOTTLE (71335-2037-8) | Jan 30, 2025 |
| 71335-2037-9 | 135 TABLET in 1 BOTTLE (71335-2037-9) | Jan 30, 2025 |
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