Gabapentin
- Product NDC
- 68071-4346
- 11-digit product format
- 680714346
- Labeler code
- 68071
- Product ID
- 68071-4346_bb7b9180-6380-9de0-e053-2a95a90a4186
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GABAPENTIN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA203244
- Marketing category
- ANDA
- Marketing start
- 2014-01-11
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 800 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4346-8 | 68071434608 | 84 TABLET, FILM COATED in 1 BOTTLE (68071-4346-8) | 2018-03-21 | 0000-00-00 | No | No | Current |
| 68071-4346-9 | 68071434609 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-4346-9) | 2018-03-21 | 0000-00-00 | No | No | Current |