Irbesartan And Hydrochlorothiazide 00093-8232
Product NDC
00093-8232- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 27, 2013
- Listing Expires
- December 31, 2027
- Application
- ANDA077369
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 12.5 mg/1 |
| Irbesartan | 300 mg/1 |
Drug Class
Angiotensin 2 Receptor Blocker [EPC]Thiazide Diuretic [EPC]Angiotensin 2 Receptor Antagonists [MoA]
Packaging Options(2)
30 TABLET, FILM COATED in 1 BOTTLE (0093-8232-56)
90 TABLET, FILM COATED in 1 BOTTLE (0093-8232-98)