NDC 65862-044
Lisinopril and Hydrochlorothiazide 20 mg / 12.5 mg tablet
On the label: Aurobindo Pharma Limited.
Where it's 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
- Hydrochlorothiazide and Lisinopril: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg / 12.5 mg
- Approval
- ANDA ANDA077606
- On the market since
- Mar 14, 2006
- Package NDCs
65862-044-0065862-044-0165862-044-0565862-044-3065862-044-99- Official label
- DailyMed (National Library of Medicine), updated Jul 21, 2026
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