Gabapentin
- Product NDC
- 60505-2551
- 11-digit product format
- 605052551
- Labeler code
- 60505
- Product ID
- 60505-2551_f73bfb89-8761-695f-0dd6-4add663ab9ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA077661
- Marketing category
- ANDA
- Marketing start
- 2006-09-15
- Marketing end
- 2020-04-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record