Gabapentin
- Product NDC
- 55154-1379
- 11-digit product format
- 551541379
- Labeler code
- 55154
- Product ID
- 55154-1379_824cd91c-4aa9-4ba8-9a07-284f172f345e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA075360
- Marketing category
- ANDA
- Marketing start
- 2005-04-06
- Marketing end
- 2019-06-30
- Substance
- GABAPENTIN
- Active strength
- 300 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