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
- 70010-743_451da3de-077d-522d-e063-6394a90a3537
- Product NDC
- 70010-743
- Form
- TABLET
- Composition / generic term
- Losartan
- Labeler
- Granules Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230308
- Source listing expiry
- 20261231
Source-listed ingredients
- LOSARTAN POTASSIUM — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (70010-743-03) · 70010-743-03
- 90 TABLET in 1 BOTTLE (70010-743-09) · 70010-743-09
- 1000 TABLET in 1 BOTTLE (70010-743-10) · 70010-743-10
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →