GABAPENTIN
- Product NDC
- 67296-2192
- 11-digit product format
- 672962192
- Labeler code
- 67296
- Product ID
- 67296-2192_44f2bb79-7a83-d8ee-e063-6394a90aa874
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Redpharm Drug
- Application
- ANDA214956
- Marketing category
- ANDA
- Marketing start
- 2021-05-10
- Substance
- GABAPENTIN
- Active strength
- 100 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6CW7F3G59X | GABAPENTIN | 60142-96-3 | GABAPENTIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67296-2192-3 | 67296219203 | 30 CAPSULE in 1 BOTTLE (67296-2192-3) | 30 capsule | 2021-05-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| GABAPENTIN | Redpharm Drug | 2025-12-02 | HUMAN PRESCRIPTION DRUG LABEL | 1 |