losartan potassium and hydrochlorothiazide (50090-4993)

Drug Facts

Product Profile

Brand Name losartan potassium and hydrochlorothiazide

Generic Name losartan potassium and hydrochlorothiazide

Labeler a-s medication solutions

Dosage Form TABLET

Routes

ORAL

Active Ingredients

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

Manufacturer

A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4993

Product ID 50090-4993_e1bcdea3-57f6-4e3c-aadc-a9204dff2f9e

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA078245

Listing Expiration 2026-12-31

Marketing Start 2010-10-06

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 500904993

Hyphenated Format 50090-4993

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 ANDA078245 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1
100 mg/1

source: ndc

Packaging

30 TABLET in 1 BOTTLE (50090-4993-0)
90 TABLET in 1 BOTTLE (50090-4993-1)
100 TABLET in 1 BOTTLE (50090-4993-2)

source: ndc

Packages (3)

50090-4993-0 30 TABLET in 1 BOTTLE (50090-4993-0) 50090-4993-1 90 TABLET in 1 BOTTLE (50090-4993-1) 50090-4993-2 100 TABLET in 1 BOTTLE (50090-4993-2)

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": "e1bcdea3-57f6-4e3c-aadc-a9204dff2f9e", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979471"], "spl_set_id": ["8a3e5be8-0a4b-48a0-817f-6e3c7674109d"], "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 in 1 BOTTLE (50090-4993-0)", "package_ndc": "50090-4993-0", "marketing_start_date": "20200406"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-4993-1)", "package_ndc": "50090-4993-1", "marketing_start_date": "20200406"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-4993-2)", "package_ndc": "50090-4993-2", "marketing_start_date": "20250930"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "50090-4993_e1bcdea3-57f6-4e3c-aadc-a9204dff2f9e", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "50090-4993", "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": "ANDA078245", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}