Zydus Lifesciences Limited
Ahmedabad, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Aug 5, 2022. 10 inspections on record, 3 with serious problems.
NDC 68084-347
Losartan Potassium 50 mg tablet, film coated
On the label: American Health Packaging.
It's a repackaged product: American Health Packaging rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-136.
Where the pills inside were made
Zydus Lifesciences Limited
Solan, India · makes it and tests it
No problems found Last FDA inspection Mar 9, 2020. 6 inspections on record.
Zydus Pharmaceuticals Limited
Matoda, India · makes it and tests it
Not inspected on record
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Losartan: see every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA078243
- On the market since
- Oct 12, 2010
- Package NDCs
68084-347-0168084-347-11- Official label
- DailyMed (National Library of Medicine), updated Jun 24, 2026
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