Gabapentin
- Product NDC
- 72189-610
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA207099
- Marketing category
- ANDA
- Substance
- GABAPENTIN
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72189-610-30 | 30 CAPSULE in 1 BOTTLE (72189-610-30) | 2025-01-27 | | No | Historical |
| 72189-610-60 | 60 CAPSULE in 1 BOTTLE (72189-610-60) | 2025-01-27 | | No | Historical |
| 72189-610-72 | 120 CAPSULE in 1 BOTTLE (72189-610-72) | 2025-01-27 | | No | Historical |
| 72189-610-90 | 90 CAPSULE in 1 BOTTLE (72189-610-90) | 2025-01-27 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Gabapentin | Direct_Rx | 2025-08-19 | HUMAN PRESCRIPTION DRUG LABEL | 4 |