Amlodipine besylate

Product NDC
71335-1397
11-digit product format
713351397
Labeler code
71335
Product ID
71335-1397_7f98291a-cf65-4bd0-9e43-fcac18900430
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amlodipine besylate
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077955
Marketing category
ANDA
Marketing start
2007-11-02
Marketing end
0000-00-00
Substance
AMLODIPINE BESYLATE
Active strength
5 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1397-0713351397005 TABLET in 1 BOTTLE (71335-1397-0) 5 tablet2007-11-020000-00-00NoNoCurrent
71335-1397-17133513970130 TABLET in 1 BOTTLE (71335-1397-1) 30 tablet2007-11-020000-00-00NoNoCurrent
71335-1397-27133513970290 TABLET in 1 BOTTLE (71335-1397-2) 90 tablet2007-11-020000-00-00NoNoCurrent
71335-1397-37133513970360 TABLET in 1 BOTTLE (71335-1397-3) 60 tablet2007-11-020000-00-00NoNoCurrent
71335-1397-471335139704100 TABLET in 1 BOTTLE (71335-1397-4) 100 tablet2007-11-020000-00-00NoNoCurrent
71335-1397-571335139705180 TABLET in 1 BOTTLE (71335-1397-5) 180 tablet2007-11-020000-00-00NoNoCurrent
71335-1397-671335139706120 TABLET in 1 BOTTLE (71335-1397-6) 120 tablet2007-11-020000-00-00NoNoCurrent
71335-1397-77133513970710 TABLET in 1 BOTTLE (71335-1397-7) 10 tablet2007-11-020000-00-00NoNoCurrent
71335-1397-871335139708500 TABLET in 1 BOTTLE (71335-1397-8) 500 tablet2007-11-020000-00-00NoNoCurrent
71335-1397-9713351397091000 TABLET in 1 BOTTLE (71335-1397-9) 1000 tablet2007-11-020000-00-00NoNoCurrent