NDC 33261-950
Losartan Potassium and Hydrochlorothiazide 100 mg / 12.5 mg tablet, film coated
On the label: Aidarex Pharmaceuticals LLC. It's repackaged: Aidarex Pharmaceuticals LLC rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-7369.
Where the pills inside were 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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Product details
- Generic drug
- Hydrochlorothiazide and Losartan: every company that makes it
- Form
- tablet, film coated
- Strength
- 100 mg / 12.5 mg
- Approval
- ANDA ANDA077157
- On the market since
- Apr 6, 2010
- Package NDCs
33261-950-3033261-950-90- Official label
- DailyMed (National Library of Medicine), updated Jan 12, 2014
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