Gabapentin
- Product NDC
- 63629-6983
- 11-digit product format
- 636296983
- Labeler code
- 63629
- Product ID
- 63629-6983_7ecd0a48-7169-430a-b77e-2221d760dc57
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075360
- Marketing category
- ANDA
- Marketing start
- 2005-04-06
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 400 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 |
|---|
| 63629-6983-1 | 63629698301 | 30 CAPSULE in 1 BOTTLE (63629-6983-1) | 30 capsule | 2016-04-26 | 0000-00-00 | No | No | Current |
| 63629-6983-2 | 63629698302 | 90 CAPSULE in 1 BOTTLE (63629-6983-2) | 90 capsule | 2016-04-26 | 0000-00-00 | No | No | Current |
| 63629-6983-3 | 63629698303 | 60 CAPSULE in 1 BOTTLE (63629-6983-3) | 60 capsule | 2016-04-26 | 0000-00-00 | No | No | Current |