Gabapentin
- Product NDC
- 63629-8060
- 11-digit product format
- 636298060
- Labeler code
- 63629
- Product ID
- 63629-8060_5c9f11d5-adce-49bc-ac73-c3db9f2d0118
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206402
- Marketing category
- ANDA
- Marketing start
- 2015-11-01
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8060-1 | 63629806001 | 90 TABLET in 1 BOTTLE (63629-8060-1) | 90 tablet | 2019-07-25 | 0000-00-00 | No | No | Current |