Gabapentin
- Product NDC
- 68001-007
- 11-digit product format
- 680010007
- Labeler code
- 68001
- Product ID
- 68001-007_c4f8a3b3-6ec7-7160-e053-2a95a90a4f77
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA078926
- Marketing category
- ANDA
- Marketing start
- 2013-07-24
- Marketing end
- 2022-02-28
- 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
- 0000-00-00
- 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 |
|---|
| 68001-007-00 | 68001000700 | 100 TABLET, FILM COATED in 1 BOTTLE (68001-007-00) | 2013-07-24 | 2022-02-28 | No | No | Current |
| 68001-007-03 | 68001000703 | 500 TABLET, FILM COATED in 1 BOTTLE (68001-007-03) | 2013-07-24 | 2022-02-28 | No | No | Current |