NDC 76420-837 – Gabapentin
Gabapentin 800 mg/1 · Tablet · Oral
Product NDC76420-837
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- Asclemed USA, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA214957
- Marketed since
- October 1, 2021
- Listing expires
- December 31, 2027
Active ingredients
- Gabapentin 800 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 76420-837-01 | 100 TABLET in 1 BOTTLE (76420-837-01) | Aug 7, 2024 |
| 76420-837-05 | 500 TABLET in 1 BOTTLE (76420-837-05) | Aug 7, 2024 |
| 76420-837-12 | 120 TABLET in 1 BOTTLE (76420-837-12) | Sep 23, 2026 |
| 76420-837-30 | 30 TABLET in 1 BOTTLE (76420-837-30) | Aug 7, 2024 |
| 76420-837-60 | 60 TABLET in 1 BOTTLE (76420-837-60) | Aug 7, 2024 |
| 76420-837-90 | 90 TABLET in 1 BOTTLE (76420-837-90) | Aug 7, 2024 |
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