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
- 29300-190_ad6e4664-08b6-4480-a1fb-6663c8024fef
- Product NDC
- 29300-190
- Form
- TABLET, FILM COATED
- Composition / generic term
- losartan potassium and hydrochlorothiazide
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170721
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROCHLOROTHIAZIDE — 12.5 mg/1
- LOSARTAN POTASSIUM — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-190-01) · 29300-190-01
- 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-190-10) · 29300-190-10
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-190-13) · 29300-190-13
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-190-19) · 29300-190-19
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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