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
- 71335-0152_d2184bfc-9552-47ce-a410-a259c0dbc7df
- Product NDC
- 71335-0152
- Form
- TABLET, FILM COATED
- 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
- 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 (71335-0152-1) · 71335-0152-1
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-0152-2) · 71335-0152-2
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-0152-3) · 71335-0152-3
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-0152-4) · 71335-0152-4
- 58 TABLET, FILM COATED in 1 BOTTLE (71335-0152-5) · 71335-0152-5
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-0152-6) · 71335-0152-6
- 180 TABLET, FILM COATED in 1 BOTTLE (71335-0152-7) · 71335-0152-7
- 1000 TABLET, FILM COATED in 1 BOTTLE (71335-0152-8) · 71335-0152-8
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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