Nateglinide

Product NDC
0615-7586
11-digit product format
006157586
Labeler code
0615
Product ID
0615-7586_9edae1d0-63c3-4a88-9902-d07722f1e930
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nateglinide
Dosage form
TABLET, COATED
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA077463
Marketing category
ANDA
Marketing start
2009-09-08
Marketing end
0000-00-00
Substance
NATEGLINIDE
Active strength
120 mg/1
Pharmacologic classes
Glinide [EPC],Potassium Channel Antagonists [MoA]
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
0615-7586-392021-07-29C16284748780-197449f38-d2ec-f6ea-e053-dbdaa90aa703f7e91323-1e7c-4c12-99aa-0959a9f6496c
0615-7586-392019-11-13C16284748780-197449f38-d2ec-f6ea-e053-dbdaa90aa703f7e91323-1e7c-4c12-99aa-0959a9f6496c