bisoprolol fumarate and hydrochlorothiazide (50090-7357)

Drug Facts

Product Profile

Brand Name bisoprolol fumarate and hydrochlorothiazide

Generic Name bisoprolol fumarate and hydrochlorothiazide

Labeler a-s medication solutions

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

bisoprolol fumarate 5 mg/1, hydrochlorothiazide 6.25 mg/1

Manufacturer

A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7357

Product ID 50090-7357_3848a437-d146-4818-8dec-6b1cdea5e9d0

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA215995

Listing Expiration 2027-12-31

Marketing Start 2022-01-26

Pharmacologic Class

Established (EPC)

thiazide diuretic [epc]

Chemical Structure

thiazides [cs]

Physiologic Effect

increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907357

Hyphenated Format 50090-7357

Supplemental Identifiers

RxCUI

854919

UNII

UR59KN573L 0J48LPH2TH

NUI

N0000175359 N0000175419 M0471776

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name bisoprolol fumarate and hydrochlorothiazide (source: ndc)

Generic Name bisoprolol fumarate and hydrochlorothiazide (source: ndc)

Application Number ANDA215995 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

5 mg/1
6.25 mg/1

source: ndc

Packaging

30 TABLET, FILM COATED in 1 BOTTLE (50090-7357-0)
90 TABLET, FILM COATED in 1 BOTTLE (50090-7357-2)

source: ndc

Packages (2)

50090-7357-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-7357-0) 50090-7357-2 90 TABLET, FILM COATED in 1 BOTTLE (50090-7357-2)

Ingredients (2)

bisoprolol fumarate (5 mg/1) hydrochlorothiazide (6.25 mg/1)

Linked Drug Pages (1)

Bisoprolol Fumarate and Hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "3848a437-d146-4818-8dec-6b1cdea5e9d0", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["UR59KN573L", "0J48LPH2TH"], "rxcui": ["854919"], "spl_set_id": ["9271a2d7-be94-4e38-9f71-41e8d55e10bc"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7357-0)", "package_ndc": "50090-7357-0", "marketing_start_date": "20241017"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7357-2)", "package_ndc": "50090-7357-2", "marketing_start_date": "20241017"}], "brand_name": "Bisoprolol Fumarate and Hydrochlorothiazide", "product_id": "50090-7357_3848a437-d146-4818-8dec-6b1cdea5e9d0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7357", "generic_name": "Bisoprolol Fumarate and Hydrochlorothiazide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate and Hydrochlorothiazide", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "6.25 mg/1"}], "application_number": "ANDA215995", "marketing_category": "ANDA", "marketing_start_date": "20220126", "listing_expiration_date": "20271231"}