losartan potassium and hydrochlorothiazide (72189-129)

Drug Facts

Product Profile

Brand Name losartan potassium and hydrochlorothiazide

Generic Name losartan potassium and hydrochlorothiazide

Labeler direct_rx

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

hydrochlorothiazide 12.5 mg/1, losartan potassium 50 mg/1

Manufacturer

Direct_Rx

Identifiers & Regulatory

Product NDC 72189-129

Product ID 72189-129_2becfaea-c7d6-ec34-e063-6294a90af5b3

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA201845

Listing Expiration 2026-12-31

Marketing Start 2020-10-15

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 72189129

Hyphenated Format 72189-129

Supplemental Identifiers

RxCUI

979464 979468 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 ANDA201845 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

12.5 mg/1
50 mg/1

source: ndc

Packaging

30 TABLET, FILM COATED in 1 BOTTLE (72189-129-30)
90 TABLET, FILM COATED in 1 BOTTLE (72189-129-90)

source: ndc

Packages (2)

72189-129-30 30 TABLET, FILM COATED in 1 BOTTLE (72189-129-30) 72189-129-90 90 TABLET, FILM COATED in 1 BOTTLE (72189-129-90)

Ingredients (2)

hydrochlorothiazide (12.5 mg/1) losartan potassium (50 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": "2becfaea-c7d6-ec34-e063-6294a90af5b3", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464", "979468", "979471"], "spl_set_id": ["8de04bf2-83dd-c494-e053-2a95a90abade"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-129-30)", "package_ndc": "72189-129-30", "marketing_start_date": "20201015"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-129-90)", "package_ndc": "72189-129-90", "marketing_start_date": "20201015"}], "brand_name": "LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE", "product_id": "72189-129_2becfaea-c7d6-ec34-e063-6294a90af5b3", "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": "72189-129", "generic_name": "losartan potassium and hydrochlorothiazide", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA201845", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}