NDC 70756-315
telmisartan and hydrochlorothiazide 40 mg / 12.5 mg tablet
On the label: Lifestar Pharma LLC..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Mankind Pharma Limited | Sirmaur, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyFeb 25, 2022 · 2 inspections |
Product details
- Generic drug
- Hydrochlorothiazide and Telmisartan: every company that makes it
- Form
- tablet, oral
- Strength
- 40 mg / 12.5 mg
- Approval
- ANDA ANDA218406
- On the market since
- Dec 25, 2025
- Package NDCs
70756-315-3070756-315-3170756-315-99- Official label
- DailyMed (National Library of Medicine), updated Aug 20, 2025
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