Gabapentin
- Product NDC
- 72162-1318
- 11-digit product format
- 721621318
- Labeler code
- 72162
- Product ID
- 72162-1318_a80b1881-b000-4369-ba1d-74058977324f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- gabapentin
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076403
- Marketing category
- ANDA
- Marketing start
- 2012-10-01
- Substance
- GABAPENTIN
- Active strength
- 250 mg/5mL
- 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 |
|---|
| 72162-1318-4 | 72162131804 | 470 mL in 1 BOTTLE (72162-1318-4) | 470 ml | 2024-11-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Gabapentin | Bryant Ranch Prepack | 2025-10-29 | HUMAN PRESCRIPTION DRUG LABEL | 102 |
| Gabapentin | Bryant Ranch Prepack | 2024-11-01 | HUMAN PRESCRIPTION DRUG LABEL | 101 |