GABAPENTIN

Product NDC
51655-379
11-digit product format
516550379
Labeler code
51655
Product ID
51655-379_92dade1a-f9a7-83c9-e053-2995a90ab833
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
GABAPENTIN
Dosage form
CAPSULE
Route
ORAL
Labeler
Northwind Pharmaceuticals
Application
ANDA090007
Marketing category
ANDA
Marketing start
2018-06-20
Marketing end
0000-00-00
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
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#