Gabapentin
- Product NDC
- 55154-3357
- 11-digit product format
- 551543357
- Labeler code
- 55154
- Product ID
- 55154-3357_d77f0adf-67c7-4e93-ab4e-aac274ae381a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA200651
- Marketing category
- ANDA
- Marketing start
- 2011-10-06
- Substance
- GABAPENTIN
- Active strength
- 600 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 | 600 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6CW7F3G59X |
| Rxcui | 310433, 310434 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55154-3357-0 | Gabapentin | 10 in 1 BAG | TABLET, FILM COATED | 10 | | 7 |
| 55154-3357-0 | Gabapentin | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55154-3357 | GABAPENTIN TABLET, FILM COATED [CARDINAL HEALTH 107, LLC] | 6 | Current NDC, Legacy NDC, 2 package rows | 20250427_b2da7d96-73ad-4f44-8784-160a384a0961.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-3357-0 | 55154335700 | 10 BLISTER PACK in 1 BAG (55154-3357-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2011-10-06 | 0000-00-00 | No | No | Current |