gabapentin
- Product NDC
- 68382-355
- 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 |
|---|
| 68382-355-01 | 100 TABLET in 1 BOTTLE (68382-355-01) | 2025-09-18 | | No | Historical |
| 68382-355-14 | 60 TABLET in 1 BOTTLE (68382-355-14) | 2025-09-18 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| gabapentin | Zydus Pharmaceuticals USA Inc. | 2025-09-05 | HUMAN PRESCRIPTION DRUG LABEL | 3 |