United States · FDA National Drug Code directory

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: 63187-918_038d5ca0-71f9-4135-9921-2e1889a9cf23
Product NDC: 63187-918
Form: TABLET, FILM COATED
Composition / generic term: Losartan Potassium and Hydrochlorothiazide
Labeler: Proficient Rx LP
Marketing category: ANDA
Marketing start / end (source format): 20160523
Source listing expiry: 20261231

Source-listed ingredients

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

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET, FILM COATED in 1 BOTTLE (63187-918-30) · 63187-918-30
60 TABLET, FILM COATED in 1 BOTTLE (63187-918-60) · 63187-918-60
90 TABLET, FILM COATED in 1 BOTTLE (63187-918-90) · 63187-918-90

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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