GABAPENTIN
- Product NDC
- 59762-4460
- 11-digit product format
- 597624460
- Labeler code
- 59762
- Product ID
- 59762-4460_ce5ad8e6-4f02-4e9b-b30a-316385755f36
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- gabapentin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Greenstone LLC
- Application
- NDA020882
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2004-03-17
- 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 |
|---|
| 59762-4460-1 | 59762446001 | 100 TABLET, FILM COATED in 1 BOTTLE (59762-4460-1) | 2019-06-03 | 0000-00-00 | No | No | Current |