NDC 61919-634
Valsartan And Hydrochlorothiazide 80 mg / 12.5 mg tablet, film coated
On the label: Direct Rx. It's repackaged from NDC 0591-2315, made by Actavis Pharma, Inc. (Valsartan 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 Valsartan: every company that makes it
- Form
- tablet, film coated
- Strength
- 80 mg / 12.5 mg
- Approval
- ANDA ANDA091519
- On the market since
- Jan 1, 2015
- Package NDCs
61919-634-3061919-634-90- Official label
- DailyMed (National Library of Medicine), updated Nov 10, 2015
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?