NDC 0093-8232
Irbesartan and Hydrochlorothiazide 300 mg / 12.5 mg tablet, film coated
On the label: Teva Pharmaceuticals USA, Inc..
Where it's 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.
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
- 300 mg / 12.5 mg
- Approval
- ANDA ANDA077369
- On the market since
- Aug 27, 2013
- Package NDCs
0093-8232-560093-8232-98- Official label
- DailyMed (National Library of Medicine), updated Jan 28, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?