Gabapentin
- Product NDC
- 68071-2463
- 11-digit product format
- 680712463
- Labeler code
- 68071
- Product ID
- 68071-2463_c5ebc9fa-5737-d249-e053-2995a90a6ca5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA205101
- Marketing category
- ANDA
- Marketing start
- 2016-02-04
- 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
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2463 | GABAPENTIN TABLET [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC | 20210630_c5ebc3e3-f7c4-9ea6-e053-2995a90a3a30.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2463-6 | 68071246306 | 60 TABLET in 1 BOTTLE (68071-2463-6) | 60 tablet | 2021-06-29 | 0000-00-00 | No | No | Current |
| 68071-2463-9 | 68071246309 | 90 TABLET in 1 BOTTLE (68071-2463-9) | 90 tablet | 2021-06-29 | 0000-00-00 | No | No | Current |