Gabapentin
- Product NDC
- 63629-8061
- 11-digit product format
- 636298061
- Labeler code
- 63629
- Product ID
- 63629-8061_3bf21373-3504-41a8-8a60-de466717177e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GABAPENTIN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203244
- Marketing category
- ANDA
- Marketing start
- 2014-01-11
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 800 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8061-1 | 63629806101 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-8061-1) | 2019-07-15 | 0000-00-00 | No | No | Current |