Gabapentin
- Product NDC
- 63629-6339
- 11-digit product format
- 636296339
- Labeler code
- 63629
- Product ID
- 63629-6339_677ec17b-59de-4eac-ad9a-16ede6498e0c
- 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
- 600 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
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 |
|---|
| 63629-6339-1 | 63629633901 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-6339-1) | 2016-09-15 | 0000-00-00 | No | No | Current |
| 63629-6339-2 | 63629633902 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-6339-2) | 2016-10-12 | 0000-00-00 | No | No | Current |