losartan potassium and hydrochlorothiazide (50090-7058)

Drug Facts

Product Profile

Brand Name losartan potassium and hydrochlorothiazide

Generic Name losartan potassium and hydrochlorothiazide

Labeler a-s medication solutions

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

hydrochlorothiazide 25 mg/1, losartan potassium 100 mg/1

Manufacturer

A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7058

Product ID 50090-7058_d5c41baf-6b10-424e-bd07-a5d916b6cd10

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA204901

Listing Expiration 2026-12-31

Marketing Start 2018-02-15

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 500907058

Hyphenated Format 50090-7058

Supplemental Identifiers

RxCUI

979471

UNII

0J48LPH2TH 3ST302B24A

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 losartan potassium and hydrochlorothiazide (source: ndc)

Generic Name losartan potassium and hydrochlorothiazide (source: ndc)

Application Number ANDA204901 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1
100 mg/1

source: ndc

Packaging

30 TABLET, FILM COATED in 1 BOTTLE (50090-7058-0)
90 TABLET, FILM COATED in 1 BOTTLE (50090-7058-1)
100 TABLET, FILM COATED in 1 BOTTLE (50090-7058-2)

source: ndc

Packages (3)

50090-7058-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-7058-0) 50090-7058-1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7058-1) 50090-7058-2 100 TABLET, FILM COATED in 1 BOTTLE (50090-7058-2)

Ingredients (2)

hydrochlorothiazide (25 mg/1) losartan potassium (100 mg/1)

Linked Drug Pages (1)

Losartan Potassium and Hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "d5c41baf-6b10-424e-bd07-a5d916b6cd10", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979471"], "spl_set_id": ["af44b2b0-1204-43c9-8ec1-d081d35b8f2b"], "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 (50090-7058-0)", "package_ndc": "50090-7058-0", "marketing_start_date": "20240116"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7058-1)", "package_ndc": "50090-7058-1", "marketing_start_date": "20240116"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-7058-2)", "package_ndc": "50090-7058-2", "marketing_start_date": "20240116"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "50090-7058_d5c41baf-6b10-424e-bd07-a5d916b6cd10", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "50090-7058", "generic_name": "losartan potassium and hydrochlorothiazide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA204901", "marketing_category": "ANDA", "marketing_start_date": "20180215", "listing_expiration_date": "20261231"}