NDC 76420-497 – Gabapentin
Gabapentin 800 mg/1 · Tablet · Oral
Product NDC76420-497
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- Asclemed USA, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA205101
- Marketed since
- February 4, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Gabapentin 800 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 76420-497-01 | 100 TABLET in 1 BOTTLE (76420-497-01) | Oct 10, 2022 |
| 76420-497-05 | 500 TABLET in 1 BOTTLE (76420-497-05) | Oct 10, 2022 |
| 76420-497-12 | 120 TABLET in 1 BOTTLE (76420-497-12) | Oct 10, 2022 |
| 76420-497-24 | 240 TABLET in 1 BOTTLE (76420-497-24) | Oct 10, 2022 |
| 76420-497-30 | 30 TABLET in 1 BOTTLE (76420-497-30) | Oct 10, 2022 |
| 76420-497-60 | 60 TABLET in 1 BOTTLE (76420-497-60) | Oct 10, 2022 |
| 76420-497-90 | 90 TABLET in 1 BOTTLE (76420-497-90) | Oct 10, 2022 |
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