NDC 71335-2819 – Gabapentin
Gabapentin 800 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-2819
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA200651
- Marketed since
- October 6, 2011
- Listing expires
- December 31, 2026
Active ingredients
- Gabapentin 800 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2819-1 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2819-1) | Oct 22, 2025 |
| 71335-2819-2 | 18 TABLET, FILM COATED in 1 BOTTLE (71335-2819-2) | Oct 22, 2025 |
| 71335-2819-3 | 58 TABLET, FILM COATED in 1 BOTTLE (71335-2819-3) | Oct 22, 2025 |
| 71335-2819-4 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2819-4) | Oct 22, 2025 |
| 71335-2819-5 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2819-5) | Oct 22, 2025 |
| 71335-2819-6 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-2819-6) | Oct 22, 2025 |
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