Gabapentin
- Product NDC
- 71335-2279
- 11-digit product format
- 713352279
- Labeler code
- 71335
- Product ID
- 71335-2279_40108b6f-b848-4fee-b4c3-55653a493b31
- 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
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Gabapentin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GABAPENTIN | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6CW7F3G59X |
| Rxcui | 310430 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2279-1 | Gabapentin | 1000 in 1 BOTTLE | CAPSULE | 1000 | | 101 |
| 71335-2279-2 | Gabapentin | 500 in 1 BOTTLE | CAPSULE | 500 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-2279 | GABAPENTIN CAPSULE [BRYANT RANCH PREPACK] | 101 | Current NDC, 2 package rows | 20240420_75418d32-6504-4cb4-b3a9-afa0eaf19b8d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2279-1 | 71335227901 | 1000 CAPSULE in 1 BOTTLE (71335-2279-1) | 1000 capsule | 2024-04-03 | No | No | Historical |
| 71335-2279-2 | 71335227902 | 500 CAPSULE in 1 BOTTLE (71335-2279-2) | 500 capsule | 2024-04-03 | No | No | Historical |