olmesartan medoxomil

Product NDC
50090-3471
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
olmesartan medoxomil
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA207662
Marketing category
ANDA
Substance
OLMESARTAN MEDOXOMIL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-3471-030 TABLET, FILM COATED in 1 BOTTLE (50090-3471-0) 2019-01-31NoHistorical
50090-3471-190 TABLET, FILM COATED in 1 BOTTLE (50090-3471-1) 2018-06-11NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
olmesartan medoxomilA-S Medication Solutions2023-11-07HUMAN PRESCRIPTION DRUG LABEL7