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
- 50090-5962_321701b0-f525-4704-ad7f-87c8bf8d01de
- Product NDC
- 50090-5962
- Form
- TABLET, FILM COATED
- Composition / generic term
- losartan potassium and hydrochlorothiazide
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20121030
- Source listing expiry
- 20261231
Source-listed ingredients
- LOSARTAN POTASSIUM — 50 mg/1
- HYDROCHLOROTHIAZIDE — 12.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET, FILM COATED in 1 BOTTLE (50090-5962-0) · 50090-5962-0
- 30 TABLET, FILM COATED in 1 BOTTLE (50090-5962-1) · 50090-5962-1
- 100 TABLET, FILM COATED in 1 BOTTLE (50090-5962-2) · 50090-5962-2
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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