NDC 61919-732
Losartan Potassium HCTZ 100 mg / 12.5 mg tablet, film coated
On the label: Direct Rx. It's repackaged from NDC 57237-208, made by Rising Pharma Holdings, 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 (it lists 1 site that repackages it). 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 Direct Rx 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 ANDA091629
- On the market since
- Apr 18, 2019
- Package NDCs
61919-732-90- Official label
- DailyMed (National Library of Medicine), updated Oct 14, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?