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
- 71335-2572_367a96b9-9983-4c67-acea-7ab1f44ea7f3
- Product NDC
- 71335-2572
- Form
- TABLET, FILM COATED
- Composition / generic term
- losartan potassium and hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180215
- 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 (71335-2572-1) · 71335-2572-1
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-2572-2) · 71335-2572-2
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-2572-3) · 71335-2572-3
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-2572-4) · 71335-2572-4
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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