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: 65862-470_194eea48-8bc8-476d-a604-4b656222d5be
Product NDC: 65862-470
Form: TABLET, FILM COATED
Composition / generic term: Losartan Potassium and Hydrochlorothiazide
Labeler: Aurobindo Pharma Limited
Marketing category: ANDA
Marketing start / end (source format): 20101006
Source listing expiry: 20261231

Source-listed ingredients

LOSARTAN POTASSIUM — 100 mg/1
HYDROCHLOROTHIAZIDE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

10 BLISTER PACK in 1 CARTON (65862-470-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 65862-470-10
30 TABLET, FILM COATED in 1 BOTTLE (65862-470-30) · 65862-470-30
5000 TABLET, FILM COATED in 1 BOTTLE (65862-470-59) · 65862-470-59
90 TABLET, FILM COATED in 1 BOTTLE (65862-470-90) · 65862-470-90
1000 TABLET, FILM COATED in 1 BOTTLE (65862-470-99) · 65862-470-99

Source and coverage

Open FDA National Drug Code directory →

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.

Browse United States records →