NDC 71205-931 – Gabapentin
Gabapentin 600 mg/1 · Tablet · Oral
Product NDC71205-931
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA205101
- Marketed since
- April 11, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Gabapentin 600 mg/1
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71205-931-00 | 100 TABLET in 1 BOTTLE (71205-931-00) | Apr 22, 2021 |
| 71205-931-30 | 30 TABLET in 1 BOTTLE (71205-931-30) | Apr 22, 2021 |
| 71205-931-55 | 500 TABLET in 1 BOTTLE (71205-931-55) | Apr 22, 2021 |
| 71205-931-60 | 60 TABLET in 1 BOTTLE (71205-931-60) | Apr 22, 2021 |
| 71205-931-64 | 240 TABLET in 1 BOTTLE (71205-931-64) | Apr 22, 2021 |
| 71205-931-67 | 270 TABLET in 1 BOTTLE (71205-931-67) | Jun 28, 2021 |
| 71205-931-72 | 120 TABLET in 1 BOTTLE (71205-931-72) | Apr 22, 2021 |
| 71205-931-76 | 360 TABLET in 1 BOTTLE (71205-931-76) | Jun 28, 2021 |
| 71205-931-78 | 180 TABLET in 1 BOTTLE (71205-931-78) | Apr 22, 2021 |
| 71205-931-90 | 90 TABLET in 1 BOTTLE (71205-931-90) | Apr 22, 2021 |
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