Gabapentin
- Product NDC
- 42495-556
- 11-digit product format
- 424950556
- Labeler code
- 42495
- Product ID
- 42495-556_cd30946c-4a89-4c53-801e-e0d1fc1c10aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Westwood Manufacturing
- Application
- ANDA075350
- Marketing category
- ANDA
- Marketing start
- 2010-01-23
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 300 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42495-556-30 | Gabapentin | 30 in 1 BLISTER PACK | CAPSULE | 30 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42495-556 | GABAPENTIN CAPSULE [WESTWOOD MANUFACTURING] | 2 | Legacy NDC, 1 package rows | 20140922_6860c072-fa85-420d-a28c-578275caed22.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 42495-556-30 | 42495055630 | 30 in 1 BLISTER PACK | Historical |