Gabapentin
- Product NDC
- 55700-386
- 11-digit product format
- 557000386
- Labeler code
- 55700
- Product ID
- 55700-386_81d745a5-24e1-4c7a-982b-1352c361bf0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GABAPENTIN
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA090007
- Marketing category
- ANDA
- Marketing start
- 2012-10-15
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 400 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