Gabapentin
- Product NDC
- 71335-2819
- 11-digit product format
- 713352819
- Labeler code
- 71335
- Product ID
- 71335-2819_08d539a0-e23e-468e-abb3-2617ec34c112
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200651
- Marketing category
- ANDA
- Marketing start
- 2011-10-06
- 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 |
|---|
| 71335-2819-1 | 71335281901 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2819-1) | 2025-10-22 | No | No | Historical |
| 71335-2819-2 | 71335281902 | 18 TABLET, FILM COATED in 1 BOTTLE (71335-2819-2) | 2025-10-22 | No | No | Historical |
| 71335-2819-3 | 71335281903 | 58 TABLET, FILM COATED in 1 BOTTLE (71335-2819-3) | 2025-10-22 | No | No | Historical |
| 71335-2819-4 | 71335281904 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2819-4) | 2025-10-22 | No | No | Historical |
| 71335-2819-5 | 71335281905 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2819-5) | 2025-10-22 | No | No | Historical |
| 71335-2819-6 | 71335281906 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-2819-6) | 2025-10-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Gabapentin | Bryant Ranch Prepack | 2025-10-22 | HUMAN PRESCRIPTION DRUG LABEL | 1 |