Gabapentin
- Product NDC
- 71335-2280
- 11-digit product format
- 713352280
- Labeler code
- 71335
- Product ID
- 71335-2280_fae067e5-38bb-499c-94a2-b0de781fd173
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206943
- Marketing category
- ANDA
- Marketing start
- 2018-05-14
- Substance
- GABAPENTIN
- Active strength
- 300 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 |
|---|
| 71335-2280-1 | 71335228001 | 1000 CAPSULE in 1 BOTTLE (71335-2280-1) | 1000 capsule | 2024-04-03 | No | No | Historical |
| 71335-2280-2 | 71335228002 | 500 CAPSULE in 1 BOTTLE (71335-2280-2) | 500 capsule | 2024-04-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Gabapentin | Bryant Ranch Prepack | 2024-04-03 | HUMAN PRESCRIPTION DRUG LABEL | 101 |