Spironolactone

Product NDC
55154-5055
11-digit product format
551545055
Labeler code
55154
Product ID
55154-5055_9572e6f6-b46c-44a0-8027-5942b02d2f86
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
spironolactone
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Cardinal Health
Application
ANDA040424
Marketing category
ANDA
Marketing start
2011-02-04
Marketing end
2020-01-31
Substance
SPIRONOLACTONE
Active strength
100 mg/1
Pharmacologic classes
Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
27O7W4T232SPIRONOLACTONE52-01-7SPIRONOLACTONE