United States · FDA National Drug Code directory

Losartan Potassium

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: 72789-029_5607a67b-6448-35cc-e063-6294a90af595
Product NDC: 72789-029
Form: TABLET, FILM COATED
Composition / generic term: Losartan Potassium
Labeler: PD-Rx Pharmaceuticals, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20150819
Source listing expiry: 20271231

Source-listed ingredients

LOSARTAN POTASSIUM — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-029-14) · 72789-029-14
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-029-30) · 72789-029-30
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-029-90) · 72789-029-90

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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