Spironolactone

Product NDC
50090-2728
11-digit product format
500902728
Labeler code
50090
Product ID
50090-2728_8f33f6bd-c039-4c70-9ec9-c6989a17e6d8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
spironolactone
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA203253
Marketing category
ANDA
Marketing start
2013-02-01
Marketing end
0000-00-00
Substance
SPIRONOLACTONE
Active strength
50 mg/1
Pharmacologic classes
Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
27O7W4T232SPIRONOLACTONE52-01-7SPIRONOLACTONE