Home NDC 0591-0841-01 NDC 0591-0841-01 - Bisoprolol Fumarate Hydrochlorothiazide This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 0591-0841
Requested NDC 0591-0841-01
Package NDCs from labels 0591-0841-01, 0591-0841-05
Manufacturer Watson Laboratories, Inc.
Effective date 2006-11-27
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0591-0841-01 Bisoprolol Fumarate Hydrochlorothiazide 100 in 1 BOTTLE TABLET, FILM COATED 100 2 0591-0841-05 Bisoprolol Fumarate Hydrochlorothiazide 500 in 1 BOTTLE TABLET, FILM COATED 500 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0591-0841 BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 2 package rows 20070105_A9630311-A5DB-4FBA-B95E-5E13AD286BC8.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Bisoprolol Fumarate ACTIVE INGREDIENT UR59KN573L BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Hydrochlorothiazide ACTIVE INGREDIENT 0J48LPH2TH BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Bisoprolol ACTIVE MOIETY Y41JS2NL6U BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Hydrochlorothiazide ACTIVE MOIETY 0J48LPH2TH BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Collodial silicon dioxide INACTIVE INGREDIENT BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Dibasic calcium phosphate INACTIVE INGREDIENT BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Hypromellose INACTIVE INGREDIENT BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Lactose monohydrate INACTIVE INGREDIENT BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Magnesium stearate INACTIVE INGREDIENT 70097M6I30 BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Microcrystalline cellulose INACTIVE INGREDIENT BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Polydextrose INACTIVE INGREDIENT BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Polyethylene glycol INACTIVE INGREDIENT BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Pregelatinized starch INACTIVE INGREDIENT BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Purified stearic acid INACTIVE INGREDIENT BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Synthetic red oxide INACTIVE INGREDIENT BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Synthetic yellow oxide INACTIVE INGREDIENT BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Titanium dioxide INACTIVE INGREDIENT 15FIX9V2JP BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2 Triacetin INACTIVE INGREDIENT XHX3C3X673 BISOPROLOL FUMARATE HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [WATSON LABORATORIES, INC.] 2
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 2 of 2 · 21 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.