Amlodipine Besylate

Product NDC
0615-6582
11-digit product format
006156582
Labeler code
0615
Product ID
0615-6582_789f7015-8b9c-4c80-98ea-71acdf80581c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amlodipine
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA076418
Marketing category
ANDA
Marketing start
2011-03-11
Marketing end
0000-00-00
Substance
AMLODIPINE BESYLATE
Active strength
3 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#