Losartan Potassium

Product NDC
61919-864
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Losartan Potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Direct Rx
Application
ANDA090083
Marketing category
ANDA
Substance
LOSARTAN POTASSIUM
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
61919-864-9090 TABLET, FILM COATED in 1 BOTTLE (61919-864-90) 2019-05-130000-00-00NoCurrent