Gabapentin
- Product NDC
- 63629-6442
- 11-digit product format
- 636296442
- Labeler code
- 63629
- Product ID
- 63629-6442_6b6189a9-c892-4d94-a288-2d03dfd0213b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200651
- Marketing category
- ANDA
- Marketing start
- 2011-10-06
- 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 |
|---|
| 63629-6442-1 | 63629644201 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-6442-1) | 2017-02-22 | 0000-00-00 | No | No | Current |
| 63629-6442-2 | 63629644202 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-6442-2) | 2016-09-16 | 0000-00-00 | No | No | Current |
| 63629-6442-3 | 63629644203 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-6442-3) | 2017-01-19 | 0000-00-00 | No | No | Current |