NDC 54868-6109
Losartan Potassium and Hydrochlorothiazide 25 mg / 100 mg tablet, film coated
On the label: Physicians Total Care, Inc.. It's repackaged: Physicians Total Care, Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-7368.
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
- 25 mg / 100 mg
- Approval
- ANDA ANDA077157
- On the market since
- Apr 19, 2010
- Package NDCs
54868-6109-054868-6109-1- Official label
- DailyMed (National Library of Medicine), updated Apr 26, 2010
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