Bisoprolol — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

BISOPROLOL FUMARATE

Base moiety

BISOPROLOL

RxNorm CUI

854901

UNII

UR59KN573L

Medication products

7

Brand names

3

Dosage forms

3

FAERS reports

209,387 · not a risk measure

Products containing this ingredient

Source: NDC Directory 7 products

Bisoprolol Fumarate Powder
11 NDC
Bisoprolol Hemifumarate Powder
1 NDC
Bisoprolol Bisoprolol fumarate · Tablet, Film Coated
Rx ANDA TE AB 7 NDC
Bisoprolol Fumarate Tablet, Film Coated
Rx ANDA TE AB 24 NDC
Bisoprolol fumarate Tablet
Rx ANDA TE AB 1 recall 18 NDC
Bisoprolol Fumarate and Hydrochlorothiazide Tablet
Rx ANDA TE AB 1 recall 12 NDC
Bisoprolol Fumarate and Hydrochlorothiazide Tablet, Film Coated
Rx ANDA TE AB 3 recalls 30 NDC

Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.

By dosage form

How this ingredient is presented across the catalogue.
Dosage form	Products	Examples
TABLET, Film Coated	3	Bisoprolol, Bisoprolol Fumarate, Bisoprolol Fumarate and Hydrochlorothiazide
Powder	2	Bisoprolol Fumarate, Bisoprolol Hemifumarate
Tablet	2	Bisoprolol fumarate, Bisoprolol Fumarate and Hydrochlorothiazide

Sources for this page

Dataset	Agency	Used for
NDC Directory	FDA	Ingredient name, strengths, products, labelers, packages
DailyMed RxNorm mappings	NLM	RxNorm concept identifier (RxCUI)
FAERS	FDA	Adverse event report totals