Gabapentin
- Product NDC
- 63629-7666
- 11-digit product format
- 636297666
- Labeler code
- 63629
- Product ID
- 63629-7666_d70a6dc6-f25d-4a9e-af25-dd2379b4c6cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077662
- Marketing category
- ANDA
- Marketing start
- 2006-04-01
- 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
- 2023-12-31
- 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 |
|---|
| 63629-7666-1 | 63629766601 | 30 TABLET in 1 BOTTLE (63629-7666-1) | 30 tablet | 2007-02-28 | 0000-00-00 | No | No | Current |
| 63629-7666-2 | 63629766602 | 60 TABLET in 1 BOTTLE (63629-7666-2) | 60 tablet | 2007-02-28 | 0000-00-00 | No | No | Current |
| 63629-7666-3 | 63629766603 | 90 TABLET in 1 BOTTLE (63629-7666-3) | 90 tablet | 2007-02-28 | 0000-00-00 | No | No | Current |
| 63629-7666-4 | 63629766604 | 120 TABLET in 1 BOTTLE (63629-7666-4) | 120 tablet | 2007-02-28 | 0000-00-00 | No | No | Current |
| 63629-7666-5 | 63629766605 | 180 TABLET in 1 BOTTLE (63629-7666-5) | 180 tablet | 2007-02-28 | 0000-00-00 | No | No | Current |
| 63629-7666-6 | 63629766606 | 270 TABLET in 1 BOTTLE (63629-7666-6) | 270 tablet | 2007-02-28 | 0000-00-00 | No | No | Current |
| 63629-7666-7 | 63629766607 | 300 TABLET in 1 BOTTLE (63629-7666-7) | 300 tablet | 2007-02-28 | 0000-00-00 | No | No | Current |
| 63629-7666-8 | 63629766608 | 500 TABLET in 1 BOTTLE (63629-7666-8) | 500 tablet | 2007-02-28 | 0000-00-00 | No | No | Current |