NDC 21695-831
Losartan Potassium And Hydrochlorothiazide 25 mg / 100 mg tablet, film coated
On the label: Rebel Distributors Corp... It's repackaged from NDC 68382-143, made by Zydus Pharmaceuticals USA Inc. (Losartan Potassium And Hydrochlorothiazide). That product's FDA listing has since ended, so its label and factories are no longer published.
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 Rebel Distributors Corp.. 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 ANDA078385
- On the market since
- Oct 4, 2010
- Package NDCs
21695-831-90- Official label
- DailyMed (National Library of Medicine), updated Apr 13, 2011
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