NDC 72162-1035
Irbesartan and Hydrochlorothiazide 150 mg / 12.5 mg tablet, film coated
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-8238.
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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Recalls
- Oct 20, 2015 · Class III · Teva Pharmaceutical Industries
Labeling: Incorrect or Missing Lot AND/OR Exp Date.
Lots: Lot #: 24I030, Exp 5/2017
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Hydrochlorothiazide and Irbesartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 150 mg / 12.5 mg
- Approval
- ANDA ANDA077369
- On the market since
- Jan 24, 2013
- Package NDCs
72162-1035-9- Official label
- DailyMed (National Library of Medicine), updated Apr 7, 2026
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