Neurontin
- Product NDC
- 58151-284
- 11-digit product format
- 581510284
- Labeler code
- 58151
- Product ID
- 58151-284_dfbc1443-0ba8-479b-8590-32bd942732d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- gabapentin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Viatris Specialty LLC
- Application
- NDA020882
- Marketing category
- NDA
- Marketing start
- 2025-10-01
- Substance
- GABAPENTIN
- Active strength
- 600 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Neurontin
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GABAPENTIN | 600 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6CW7F3G59X |
| Rxcui | 105028, 105029, 105030, 261280, 261281, 283523, 310430, 310431, 310432, 310433, 310434, 351973 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 58151-284-01 | Neurontin | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 47 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58151-284 | NEURONTIN (GABAPENTIN) CAPSULE NEURONTIN (GABAPENTIN) TABLET, FILM COATED NEURONTIN (GABAPENTIN) SOLUTION [VIATRIS SPECIALTY LLC] | 41 | Current NDC, 1 package rows | 20250521_97935fd9-1d4a-43b6-a5d9-de994591187b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 58151-284-01 | 58151028401 | 100 TABLET, FILM COATED in 1 BOTTLE (58151-284-01) | 2025-10-01 | No | No | Current |