GABAPENTIN
- Product NDC
- 71335-3109
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211314
- Marketing category
- ANDA
- Substance
- GABAPENTIN
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 71335-3109-1 | 500 CAPSULE in 1 BOTTLE (71335-3109-1) | 2026-03-30 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| These highlights do not include all the information needed to use GABAPENTIN CAPSULES safely and effectively. See full prescribing information for GABAPENTIN CAPSULES. GABAPENTIN capsules, for oral use Initial U.S. Approval: 1993 | Bryant Ranch Prepack | 2026-03-30 | HUMAN PRESCRIPTION DRUG LABEL | 1 |