Gabapentin
- Product NDC
- 63629-7962
- 11-digit product format
- 636297962
- Labeler code
- 63629
- Product ID
- 63629-7962_805708a6-ad03-46dd-95d0-1203319b39dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078428
- Marketing category
- ANDA
- Marketing start
- 2009-11-24
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 300 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 |
|---|
| 63629-7962-1 | 63629796201 | 30 CAPSULE in 1 BOTTLE (63629-7962-1) | 30 capsule | 2019-03-13 | 0000-00-00 | No | No | Current |
| 63629-7962-2 | 63629796202 | 90 CAPSULE in 1 BOTTLE (63629-7962-2) | 90 capsule | 2019-03-13 | 0000-00-00 | No | No | Current |