NDC 68788-6452
Losartan Potassium and Hydrochlorothiazide 25 mg / 100 mg tablet, film coated
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Aurobindo Pharma Limited's NDC 65862-470.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Mahabubnagar, India | Makes it and tests it | No problems foundJan 18, 2023 · 2 inspections |
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · repackages it
Product details
- Generic drug
- Hydrochlorothiazide and Losartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 25 mg / 100 mg
- Approval
- ANDA ANDA091629
- On the market since
- Aug 5, 2016
- Package NDCs
68788-6452-168788-6452-368788-6452-668788-6452-9- Official label
- DailyMed (National Library of Medicine), updated Aug 4, 2025
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