SPIRONOLACTONE

Product NDC
76420-558
11-digit product format
764200558
Labeler code
76420
Product ID
76420-558_f8b9eb31-4486-7638-e053-6394a90aee92
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
SPIRONOLACTONE
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA089424
Marketing category
ANDA
Marketing start
1986-07-23
Substance
SPIRONOLACTONE
Active strength
100 mg/1
Pharmacologic classes
Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
27O7W4T232SPIRONOLACTONE52-01-7SPIRONOLACTONE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
76420-558-0176420055801100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-558-01) 2023-04-07NoNoHistorical
76420-558-307642005583030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-558-30) 2023-04-07NoNoHistorical
76420-558-607642005586060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-558-60) 2023-04-07NoNoHistorical
76420-558-907642005589090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-558-90) 2023-04-07NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
SPIRONOLACTONEAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2023-04-07HUMAN PRESCRIPTION DRUG LABEL1