Gabapentin
- Product NDC
- 50090-7400
- 11-digit product format
- 500907400
- Labeler code
- 50090
- Product ID
- 50090-7400_7216f0b3-5a46-4015-ac99-6327e840fb69
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA207057
- Marketing category
- ANDA
- Marketing start
- 2021-11-01
- Substance
- GABAPENTIN
- Active strength
- 800 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7400-0 | 50090740000 | 60 TABLET, COATED in 1 BOTTLE (50090-7400-0) | 2024-10-24 | No | No | Historical |
| 50090-7400-1 | 50090740001 | 90 TABLET, COATED in 1 BOTTLE (50090-7400-1) | 2024-10-24 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Gabapentin | A-S Medication Solutions | 2025-11-19 | HUMAN PRESCRIPTION DRUG LABEL | 3 |