NDC 0093-8232-56
Irbesartan and Hydrochlorothiazide 12.5 mg/1
Irbesartan and Hydrochlorothiazide · TABLET, FILM COATED
Irbesartan and Hydrochlorothiazide is a tablet, film coated containing irbesartan and hydrochlorothiazide at a strength of 12.5 mg/1. Manufactured by Teva Pharmaceuticals USA, Inc..
Key Facts
- Brand Name
- Irbesartan and Hydrochlorothiazide
- Generic Name
- Irbesartan and Hydrochlorothiazide
- NDC Code (Package)
0093-8232-56- NDC Code (Product)
0093-8232- Manufacturer
- Teva Pharmaceuticals USA, Inc.
- Strength
- 12.5 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA077369
- Drug Class
- Thiazide Diuretic [EPC]; Angiotensin 2 Receptor Blocker [EPC]
- Marketing Start
- 08/27/2013
Recall History
No Recall HistoryView Full Drug Page
Irbesartan and Hydrochlorothiazide — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.