NDC 54868-6440
Valsartan and Hydrochlorothiazide 320 mg / 12.5 mg tablet, film coated
On the label: Physicians Total Care, Inc.. It's repackaged from NDC 0781-5951, made by Sandoz 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 and relabels 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 Physicians Total Care, Inc. names for other drugs.
Product details
- Generic drug
- Hydrochlorothiazide and Valsartan: every company that makes it
- Form
- tablet, film coated
- Strength
- 320 mg / 12.5 mg
- Approval
- NDA AUTHORIZED GENERIC NDA020818
- On the market since
- Dec 1, 2014
- Package NDCs
54868-6440-0- Official label
- DailyMed (National Library of Medicine), updated May 7, 2015
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