NDC 16714-332 – Gabapentin
Gabapentin 800 mg/1 · Tablet, Film Coated · Oral
Product NDC16714-332
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- NorthStar Rx LLC
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 16714-332-01 | 100 TABLET, FILM COATED in 1 BOTTLE (16714-332-01) | Oct 6, 2011 |
| 16714-332-02 | 500 TABLET, FILM COATED in 1 BOTTLE (16714-332-02) | Oct 6, 2011 |
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