Irbesartan And Hydrochlorothiazide 71335-1097
Product NDC
71335-1097- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 24, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA077369
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 12.5 mg/1 |
| Irbesartan | 150 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin 2 Receptor Blocker [EPC]Angiotensin 2 Receptor Antagonists [MoA]
Packaging Options(3)
30 TABLET, FILM COATED in 1 BOTTLE (71335-1097-1)
90 TABLET, FILM COATED in 1 BOTTLE (71335-1097-2)
28 TABLET, FILM COATED in 1 BOTTLE (71335-1097-3)