NDC 68180-194
Telmisartan and Hydrochlorothiazide 80 mg / 12.5 mg tablet
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Lupin Pharmaceuticals, Inc. names for other drugs.
Product details
- Generic drug
- Hydrochlorothiazide and Telmisartan: every company that makes it
- Form
- tablet, oral
- Strength
- 80 mg / 12.5 mg
- Approval
- ANDA ANDA091351
- On the market since
- Aug 7, 2014
- Package NDCs
68180-194-0668180-194-0968180-194-11- Official label
- DailyMed (National Library of Medicine), updated Jan 19, 2024
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