spironolactone

Product NDC
71335-1586
11-digit product format
713351586
Labeler code
71335
Product ID
71335-1586_672bd23f-94be-43d0-9dcf-ba691c71c6f2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
spironolactone
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA205936
Marketing category
ANDA
Marketing start
2018-08-15
Marketing end
0000-00-00
Substance
SPIRONOLACTONE
Active strength
100 mg/1
Pharmacologic classes
Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1586-171335158601100 TABLET in 1 BOTTLE (71335-1586-1) 100 tablet2020-04-290000-00-00NoNoCurrent
71335-1586-2713351586023 TABLET in 1 BOTTLE (71335-1586-2) 3 tablet2020-04-290000-00-00NoNoCurrent
71335-1586-37133515860330 TABLET in 1 BOTTLE (71335-1586-3) 30 tablet2020-04-290000-00-00NoNoCurrent
71335-1586-47133515860490 TABLET in 1 BOTTLE (71335-1586-4) 90 tablet2020-04-290000-00-00NoNoCurrent
71335-1586-57133515860560 TABLET in 1 BOTTLE (71335-1586-5) 60 tablet2020-04-290000-00-00NoNoCurrent