NDC 76282-406 – Gabapentin
Gabapentin 800 mg/1 · Tablet, Film Coated · Oral
Product NDC76282-406
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- Exelan Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202764
- Marketed since
- November 2, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Gabapentin 800 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 76282-406-01 | 100 TABLET, FILM COATED in 1 BOTTLE (76282-406-01) | Nov 2, 2012 |
| 76282-406-05 | 500 TABLET, FILM COATED in 1 BOTTLE (76282-406-05) | Nov 2, 2012 |
| 76282-406-30 | 30 TABLET, FILM COATED in 1 BOTTLE (76282-406-30) | Nov 2, 2012 |
| 76282-406-90 | 90 TABLET, FILM COATED in 1 BOTTLE (76282-406-90) | Nov 2, 2012 |
Recalls mentioning this NDC
- D-1272-2020 May 27, 2020 · Class III
Failed Impurities/Degradation Specifications; failure of Impurity A test at the 12-month long-term stability testing.
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