NDC 71335-1041 – Gabapentin
Gabapentin 800 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1041
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203244
- Marketed since
- January 11, 2014
- Listing expires
- December 31, 2026
Active ingredients
- Gabapentin 800 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1041-1 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1041-1) | Jan 29, 2019 |
| 71335-1041-2 | 18 TABLET, FILM COATED in 1 BOTTLE (71335-1041-2) | Apr 2, 2024 |
| 71335-1041-3 | 58 TABLET, FILM COATED in 1 BOTTLE (71335-1041-3) | Apr 2, 2024 |
| 71335-1041-4 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1041-4) | Apr 28, 2020 |
| 71335-1041-5 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1041-5) | Apr 8, 2019 |
| 71335-1041-6 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1041-6) | Dec 27, 2018 |
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