Amlodipine and olmesartan medoxomil

Product NDC
59746-526
11-digit product format
597460526
Labeler code
59746
Product ID
59746-526_660f89b1-ff32-4d61-aa48-56d9e6c15dce
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amlodipine and olmesartan medoxomil
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Jubilant Cadista Pharmaceuticals Inc.
Application
ANDA207450
Marketing category
ANDA
Marketing start
2017-05-15
Marketing end
0000-00-00
Substance
AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
Active strength
5 mg/1; mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
59746-526-0159746052601100 TABLET, FILM COATED in 1 BOTTLE (59746-526-01) 2017-05-150000-00-00NoNoCurrent
59746-526-10597460526101000 TABLET, FILM COATED in 1 BOTTLE (59746-526-10) 2017-05-150000-00-00NoNoCurrent
59746-526-305974605263030 TABLET, FILM COATED in 1 BOTTLE (59746-526-30) 2017-05-150000-00-00NoNoCurrent
59746-526-905974605269090 TABLET, FILM COATED in 1 BOTTLE (59746-526-90) 2017-05-150000-00-00NoNoCurrent