United States · FDA National Drug Code directory

Losartan potassium Tablets, 100 mg

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
59746-335_cfcfa1c5-48d3-4370-aa10-e1d054c1844f
Product NDC
59746-335
Form
TABLET
Composition / generic term
losartan potassium
Labeler
Jubilant Cadista Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20120918
Source listing expiry
20271231

Source-listed ingredients

  • LOSARTAN POTASSIUM — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (59746-335-01) · 59746-335-01
  • 1000 TABLET in 1 BOTTLE (59746-335-10) · 59746-335-10
  • 30 TABLET in 1 BOTTLE (59746-335-30) · 59746-335-30
  • 90 TABLET in 1 BOTTLE (59746-335-90) · 59746-335-90

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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