Gabapentin
- Product NDC
- 67046-1536
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Coupler LLC
- Application
- ANDA205101
- Marketing category
- ANDA
- Substance
- GABAPENTIN
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 67046-1536-3 | 30 TABLET in 1 BLISTER PACK (67046-1536-3) | 2025-03-25 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Gabapentin | Coupler LLC | 2025-03-25 | HUMAN PRESCRIPTION DRUG LABEL | 1 |