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
- 71335-2558_db6c4965-367c-4960-a33d-4975be838cfa
- Product NDC
- 71335-2558
- Form
- TABLET
- Composition / generic term
- Losartan Potassium and Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20101006
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROCHLOROTHIAZIDE — 25 mg/1
- LOSARTAN POTASSIUM — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-2558-1) · 71335-2558-1
- 90 TABLET in 1 BOTTLE (71335-2558-2) · 71335-2558-2
- 60 TABLET in 1 BOTTLE (71335-2558-3) · 71335-2558-3
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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