NDC 63304-538
Lisinopril and Hydrochlorothiazide 20 mg / 25 mg tablet
On the label: Ranbaxy Laboratories Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Cambrex Profarmaco Milano SRL | Paullo, Italy | Makes the active ingredient | No problems foundNov 11, 2022 · 7 inspections, 1 with FDA action |
| Matrix Pharmacorp Private Limited | Hyderabad, India | Makes the active ingredient | Problems found, fixed voluntarilyNov 28, 2025 · 6 inspections |
| Ohm Laboratories Inc. | North Brunswick, NJ, United States | Makes it and packages it | No problems foundOct 31, 2024 · 22 inspections |
| Ranbaxy laboratories Limited Toansa | Location not on file | Makes the active ingredient | Not inspected on record |
Product details
- Generic drug
- Hydrochlorothiazide and Lisinopril: every company that makes it
- Form
- tablet
- Strength
- 20 mg / 25 mg
- Approval
- ANDA ANDA076007
- On the market since
- Jul 2, 2002
- Package NDCs
63304-538-0163304-538-05- Official label
- DailyMed (National Library of Medicine), updated Dec 5, 2013
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