Gabapentin
- Product NDC
- 68788-9923
- 11-digit product format
- 687889923
- Labeler code
- 68788
- Product ID
- 68788-9923_51bd1139-d6cd-445b-b561-00a35a82a51e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA200651
- Marketing category
- ANDA
- Marketing start
- 2012-01-27
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record