Gabapentin
- Product NDC
- 50090-7673
- 11-digit product format
- 500907673
- Labeler code
- 50090
- Product ID
- 50090-7673_01196905-4565-450b-8c37-8ed986ed3adb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA204989
- Marketing category
- ANDA
- Marketing start
- 2016-02-18
- 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 |
|---|
| 50090-7673-0 | 50090767300 | 90 CAPSULE in 1 BOTTLE (50090-7673-0) | 90 capsule | 2025-10-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Gabapentin | A-S Medication Solutions | 2025-10-10 | HUMAN PRESCRIPTION DRUG LABEL | 1 |