NDC 71335-1392
Irbesartan and Hydrochlorothiazide 150 mg / 12.5 mg tablet, film coated
On the label: Bryant Ranch Prepack. It's repackaged from NDC 0955-1045, made by Sanofi-Aventis U.S. LLC (Irbesartan 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 Bryant Ranch Prepack names for other drugs.
Product details
- Generic drug
- Hydrochlorothiazide and Irbesartan: every company that makes it
- Form
- tablet, film coated
- Strength
- 150 mg / 12.5 mg
- Approval
- NDA authorized generic NDA020758
- On the market since
- Sep 30, 2019
- Package NDCs
71335-1392-171335-1392-271335-1392-3- Official label
- DailyMed (National Library of Medicine), updated May 20, 2024
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