NDC 33261-818
Losortan Potassium 50 mg tablet, film coated
On the label: Aidarex Pharmaceuticals LLC. It's repackaged: Aidarex Pharmaceuticals LLC rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-136.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
| Zydus Lifesciences Limited | Solan, India | Makes it and tests it | No problems foundMar 9, 2020 · 6 inspections |
| Zydus Pharmaceuticals Limited | Matoda, India | Makes it and tests it | Not inspected on record |
Product details
- Generic drug
- Losartan: every company that makes it
- Form
- tablet, film coated
- Strength
- 50 mg
- Approval
- ANDA ANDA078243
- On the market since
- Oct 4, 2010
- Package NDCs
33261-818-3033261-818-6033261-818-90- Official label
- DailyMed (National Library of Medicine), updated Jan 11, 2014
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