gabapentin
- Product NDC
- 68382-608
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA203934
- Marketing category
- ANDA
- Substance
- GABAPENTIN
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68382-608-05 | 500 TABLET in 1 BOTTLE (68382-608-05) | 2024-01-25 | | No | Historical |
| 68382-608-16 | 90 TABLET in 1 BOTTLE (68382-608-16) | 2024-01-25 | | No | Historical |
| 68382-608-77 | 10 BLISTER PACK in 1 CARTON (68382-608-77) / 10 TABLET in 1 BLISTER PACK (68382-608-30) | 2024-01-25 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| gabapentin | Zydus Pharmaceuticals USA Inc. | 2025-09-05 | HUMAN PRESCRIPTION DRUG LABEL | 3 |