spironolactone

Product NDC
71335-1604
11-digit product format
713351604
Labeler code
71335
Product ID
71335-1604_f3c7fbe8-0edc-4f16-b0cb-3548c018ac93
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
25 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
71335-1604-17133516040130 TABLET in 1 BOTTLE (71335-1604-1) 30 tablet2018-08-150000-00-00NoNoCurrent
71335-1604-27133516040260 TABLET in 1 BOTTLE (71335-1604-2) 60 tablet2018-08-150000-00-00NoNoCurrent
71335-1604-37133516040390 TABLET in 1 BOTTLE (71335-1604-3) 90 tablet2018-08-150000-00-00NoNoCurrent
71335-1604-47133516040414 TABLET in 1 BOTTLE (71335-1604-4) 14 tablet2018-08-150000-00-00NoNoCurrent
71335-1604-571335160405100 TABLET in 1 BOTTLE (71335-1604-5) 100 tablet2018-08-150000-00-00NoNoCurrent
71335-1604-6713351604067 TABLET in 1 BOTTLE (71335-1604-6) 7 tablet2018-08-150000-00-00NoNoCurrent
71335-1604-77133516040710 TABLET in 1 BOTTLE (71335-1604-7) 10 tablet2022-02-100000-00-00NoNoCurrent