Bisoprolol

Product NDC
72162-2177
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Bisoprolol fumarate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA075474
Marketing category
ANDA
Substance
BISOPROLOL FUMARATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72162-2177-1100 TABLET, FILM COATED in 1 BOTTLE (72162-2177-1) 2023-12-07NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Bisoprolol Tablets USP 5mg and 10mgBryant Ranch Prepack2023-12-07HUMAN PRESCRIPTION DRUG LABEL100