Gabapentin
- Product NDC
- 68071-1292
- 11-digit product format
- 680711292
- Labeler code
- 68071
- Product ID
- 68071-1292_bb04dd0d-7dfc-15be-e053-2995a90a037e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA077662
- Marketing category
- ANDA
- Marketing start
- 2006-04-01
- 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-1292-2 | 68071129202 | 120 TABLET in 1 BOTTLE (68071-1292-2) | 120 tablet | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68071-1292-3 | 68071129203 | 30 TABLET in 1 BOTTLE (68071-1292-3) | 30 tablet | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68071-1292-4 | 68071129204 | 14 TABLET in 1 BOTTLE (68071-1292-4) | 14 tablet | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68071-1292-6 | 68071129206 | 60 TABLET in 1 BOTTLE (68071-1292-6) | 60 tablet | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68071-1292-7 | 68071129207 | 7 TABLET in 1 BOTTLE (68071-1292-7) | 7 tablet | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68071-1292-8 | 68071129208 | 84 TABLET in 1 BOTTLE (68071-1292-8) | 84 tablet | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68071-1292-9 | 68071129209 | 90 TABLET in 1 BOTTLE (68071-1292-9) | 90 tablet | 2017-02-22 | 0000-00-00 | No | No | Current |