Gabapentin

Product NDC
0615-6554
11-digit product format
006156554
Labeler code
0615
Product ID
0615-6554_10e4f6c8-1929-4ef3-8dfc-8026dea48ae1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA075694
Marketing category
ANDA
Marketing start
2004-10-21
Marketing end
0000-00-00
Substance
GABAPENTIN
Active strength
800 mg/1
Pharmacologic classes
Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0615-6554-392021-05-06C16284748780-19d75b9d0-7abf-f424-e053-dadaa90a57ce236ecbbb-16a3-404b-b6de-5308c641c1a0
0615-6554-392020-01-31C16284748780-19d75b9d0-7abf-f424-e053-dadaa90a57ce236ecbbb-16a3-404b-b6de-5308c641c1a0