Spironolactone

Product NDC
55700-968
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
spironolactone
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Quality Care Products, LLC
Application
ANDA203512
Marketing category
ANDA
Substance
SPIRONOLACTONE
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
55700-968-3030 TABLET, FILM COATED in 1 BOTTLE (55700-968-30) 2022-07-130000-00-00NoCurrent