Gabapentin
- Product NDC
- 72162-2138
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206943
- Marketing category
- ANDA
- Substance
- GABAPENTIN
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72162-2138-1 | 100 CAPSULE in 1 BOTTLE, PLASTIC (72162-2138-1) | 2023-10-12 | | No | Historical |
| 72162-2138-5 | 500 CAPSULE in 1 BOTTLE, PLASTIC (72162-2138-5) | 2023-10-12 | | No | Historical |
| 72162-2138-9 | 90 CAPSULE in 1 BOTTLE, PLASTIC (72162-2138-9) | 2023-10-12 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Gabapentin | Bryant Ranch Prepack | 2024-10-18 | HUMAN PRESCRIPTION DRUG LABEL | 102 |