Losartan Potassium

Product NDC
63629-8087
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Losartan Potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA090083
Marketing category
ANDA
Substance
LOSARTAN POTASSIUM
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
63629-8087-190 TABLET, FILM COATED in 1 BOTTLE (63629-8087-1) 2019-07-250000-00-00NoCurrent
63629-8087-230 TABLET, FILM COATED in 1 BOTTLE (63629-8087-2) 2019-07-250000-00-00NoCurrent