NDC 0597-0042
Micardis HCT 25 mg / 80 mg tablet
On the label: Boehringer Ingelheim Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Boehringer Ingelheim Pharma GmbH and Co. KG | Ingelheim am Rhein, Germany | Makes it, packages it and labels it | Problems found, fixed voluntarilyMay 15, 2025 · 8 inspections, 1 with FDA action |
| Rottendorf Pharma GmbH | Ennigerloh, Germany | Makes it, packages it and labels it | Problems found, fixed voluntarilyMar 14, 2024 · 6 inspections |
| Boehringer Ingelheim Promeco S.A. de C.V. | Mexico City, Mexico | Packages it and labels it | Problems found, fixed voluntarilyMay 20, 2022 · 5 inspections, 1 with FDA action |
| Sixarp, LLC | Grand Rapids, MI, United States | Packages it and labels it | No problems foundMar 6, 2025 · 4 inspections |
Product details
- Generic drug
- Hydrochlorothiazide and Telmisartan: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg / 80 mg
- Approval
- NDA NDA021162
- On the market since
- Dec 1, 2000
- Package NDCs
0597-0042-37- Official label
- DailyMed (National Library of Medicine), updated Dec 31, 2024
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