NDC 70518-2323 – Gabapentin
Gabapentin 800 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-2323
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA200651
- Marketed since
- September 24, 2019
- Listing expires
- December 31, 2027
Active ingredients
- Gabapentin 800 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 70518-2323-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2323-0) | Sep 24, 2019 |
| 70518-2323-1 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2323-1) | Oct 4, 2019 |
| 70518-2323-2 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2323-2) | Oct 9, 2019 |
| 70518-2323-3 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2323-3) | Dec 23, 2020 |
| 70518-2323-4 | 100 POUCH in 1 BOX (70518-2323-4) / 1 TABLET, FILM COATED in 1 POUCH (70518-2323-5) | Mar 24, 2026 |
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