GABAPENTIN
- Product NDC
- 68071-3759
- 11-digit product format
- 680713759
- Labeler code
- 68071
- Product ID
- 68071-3759_2b396658-c84e-4d36-e063-6394a90afe02
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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 |
|---|
| 68071-3759-1 | 68071375901 | 100 CAPSULE in 1 BOTTLE (68071-3759-1) | 100 capsule | 2025-01-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| GABAPENTIN | NuCare Pharmaceuticals,Inc. | 2025-01-08 | HUMAN PRESCRIPTION DRUG LABEL | 1 |