Losartan Potassium

Product NDC
50090-2882
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Losartan Potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA090083
Marketing category
ANDA
Substance
LOSARTAN POTASSIUM
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-2882-030 TABLET, FILM COATED in 1 BOTTLE (50090-2882-0) 2017-04-260000-00-00NoCurrent
50090-2882-190 TABLET, FILM COATED in 1 BOTTLE (50090-2882-1) 2017-02-220000-00-00NoCurrent

Related DailyMed Labels