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losartan potassium and hydrochlorothiazide

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 72162-2461_1c647f86-de31-4e1b-84c2-5a3d15bc1c70
Product NDC: 72162-2461
Form: TABLET, FILM COATED
Composition / generic term: losartan potassium and hydrochlorothiazide
Labeler: Bryant Ranch Prepack
Marketing category: ANDA
Marketing start / end (source format): 20170721
Source listing expiry: 20261231

Source-listed ingredients

HYDROCHLOROTHIAZIDE — 12.5 mg/1
LOSARTAN POTASSIUM — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1000 TABLET, FILM COATED in 1 BOTTLE (72162-2461-0) · 72162-2461-0
30 TABLET, FILM COATED in 1 BOTTLE (72162-2461-3) · 72162-2461-3
90 TABLET, FILM COATED in 1 BOTTLE (72162-2461-9) · 72162-2461-9

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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