NDC 70518-0245
Losartan Potassium 50 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-202.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Losartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA090083
- On the market since
- Feb 21, 2017
- Package NDCs
70518-0245-070518-0245-170518-0245-2- Official label
- DailyMed (National Library of Medicine), updated Jun 24, 2026
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