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
- 43547-424_0be72eb2-c56a-4721-8cb5-d9b778c3e179
- Product NDC
- 43547-424
- Form
- TABLET, FILM COATED
- Composition / generic term
- losartan potassium and hydrochlorothiazide
- Labeler
- Solco Healthcare US, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180215
- Source listing expiry
- 20271231
Source-listed ingredients
- LOSARTAN POTASSIUM — 100 mg/1
- HYDROCHLOROTHIAZIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (43547-424-03) · 43547-424-03
- 90 TABLET, FILM COATED in 1 BOTTLE (43547-424-09) · 43547-424-09
- 1000 TABLET, FILM COATED in 1 BOTTLE (43547-424-11) · 43547-424-11
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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