LOSARTAN POTASSIUM

Product NDC
13107-195
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
LOSARTAN POTASSIUM
Dosage form
TABLET
Route
ORAL
Labeler
Aurolife Pharma, LLC
Application
ANDA090083
Marketing category
ANDA
Substance
LOSARTAN POTASSIUM
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
13107-195-05500 TABLET in 1 BOTTLE (13107-195-05) 2010-10-060000-00-00NoCurrent
13107-195-3030 TABLET in 1 BOTTLE (13107-195-30) 2010-10-060000-00-00NoCurrent
13107-195-9090 TABLET in 1 BOTTLE (13107-195-90) 2010-10-060000-00-00NoCurrent
13107-195-991000 TABLET in 1 BOTTLE (13107-195-99) 2010-10-060000-00-00NoCurrent

Related DailyMed Labels