NDC 31722-755
Losartan Potassium And Hydrochlorothiazide 50 mg / 12.5 mg tablet, film coated
On the label: Camber Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hetero Labs Limited | Mahabubnagar, India | Makes it | Problems found, fixed voluntarilyAug 12, 2022 · 5 inspections, 1 with FDA action |
Product details
- Generic drug
- Hydrochlorothiazide and Losartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg / 12.5 mg
- Approval
- ANDA ANDA219869
- On the market since
- May 27, 2026
- Package NDCs
31722-755-1031722-755-3031722-755-90- Official label
- DailyMed (National Library of Medicine), updated Jun 9, 2026
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