gabapentin
- Product NDC
- 71335-1018
- 11-digit product format
- 713351018
- Labeler code
- 71335
- Product ID
- 71335-1018_07178f05-de42-4231-8b1f-4a976b8b5614
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- gabapentin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077525
- Marketing category
- ANDA
- Marketing start
- 2006-08-24
- 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
- 2021-12-31
- 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 |
|---|
| 71335-1018-1 | 71335101801 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1018-1) | 2010-02-26 | 0000-00-00 | No | No | Current |
| 71335-1018-2 | 71335101802 | 18 TABLET, FILM COATED in 1 BOTTLE (71335-1018-2) | 2010-02-26 | 0000-00-00 | No | No | Current |
| 71335-1018-3 | 71335101803 | 58 TABLET, FILM COATED in 1 BOTTLE (71335-1018-3) | 2010-02-26 | 0000-00-00 | No | No | Current |
| 71335-1018-4 | 71335101804 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1018-4) | 2010-02-26 | 0000-00-00 | No | No | Current |
| 71335-1018-5 | 71335101805 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1018-5) | 2010-02-26 | 0000-00-00 | No | No | Current |
| 71335-1018-6 | 71335101806 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1018-6) | 2010-02-26 | 0000-00-00 | No | No | Current |