Gabapentin
- Product NDC
- 68788-7005
- 11-digit product format
- 687887005
- Labeler code
- 68788
- Product ID
- 68788-7005_e4432867-826b-4c66-8bd8-ed29648bcbd7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GABAPENTIN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA203244
- Marketing category
- ANDA
- Marketing start
- 2017-08-11
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7005-1 | 68788700501 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7005-1) | 2017-08-11 | 0000-00-00 | No | No | Current |
| 68788-7005-3 | 68788700503 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7005-3) | 2017-08-11 | 0000-00-00 | No | No | Current |
| 68788-7005-6 | 68788700506 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7005-6) | 2017-08-11 | 0000-00-00 | No | No | Current |
| 68788-7005-8 | 68788700508 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-7005-8) | 2017-08-11 | 0000-00-00 | No | No | Current |
| 68788-7005-9 | 68788700509 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7005-9) | 2017-08-11 | 0000-00-00 | No | No | Current |