Gabapentin
- Product NDC
- 67046-227
- 11-digit product format
- 670460227
- Labeler code
- 67046
- Product ID
- 67046-227_33b9c9ba-f71c-49f9-9bfc-f0d8a68aeab6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA077662
- Marketing category
- ANDA
- Marketing start
- 2009-08-30
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 600 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 |
|---|
| 67046-227-30 | Gabapentin | 30 in 1 BLISTER PACK | TABLET | 30 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-227 | GABAPENTIN TABLET [CONTRACT PHARMACY SERVICES-PA] | 2 | Legacy NDC, 1 package rows | 20100820_2f45060b-ce5c-4869-87c0-fd7d2224e86c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67046-227-30 | 67046022730 | 30 in 1 BLISTER PACK | Historical |