Gabapentin
- Product NDC
- 63629-6791
- 11-digit product format
- 636296791
- Labeler code
- 63629
- Product ID
- 63629-6791_1e027c7f-f3e1-4898-8ad3-5bddd8a7d29e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078787
- Marketing category
- ANDA
- Marketing start
- 2008-01-31
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 100 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6791-1 | 63629679101 | 60 CAPSULE in 1 BOTTLE (63629-6791-1) | 60 capsule | 2015-09-22 | 0000-00-00 | No | No | Current |
| 63629-6791-2 | 63629679102 | 90 CAPSULE in 1 BOTTLE (63629-6791-2) | 90 capsule | 2015-09-22 | 0000-00-00 | No | No | Current |