NDC 68645-412
Losartan Potassium and Hydrochlorothiazide 50 mg / 12.5 mg tablet, film coated
On the label: Legacy Pharmaceutical Packaging. It's repackaged from NDC 60505-2915, made by Apotex Corp. (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 Legacy Pharmaceutical Packaging names for other drugs.
Product details
- Generic drug
- Hydrochlorothiazide and Losartan: every company that makes it
- Form
- tablet, film coated
- Strength
- 50 mg / 12.5 mg
- Approval
- ANDA ANDA090150
- On the market since
- Oct 6, 2010
- Package NDCs
68645-412-70- Official label
- DailyMed (National Library of Medicine), updated Oct 17, 2012
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