Losartan potassium

Product NDC
67046-1470
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Losartan potassium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Coupler LLC
Application
ANDA217396
Marketing category
ANDA
Substance
LOSARTAN POTASSIUM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
67046-1470-330 TABLET, FILM COATED in 1 BLISTER PACK (67046-1470-3) 2025-02-04NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Losartan potassiumCoupler LLC2025-02-04HUMAN PRESCRIPTION DRUG LABEL1