Fosinopril Sodium And Hydrochlorothiazide 65862-0308-99
- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 9, 2009
- Listing Expires
- December 31, 2026
- Application
- ANDA079245
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fosinopril Sodium | 10 mg/1 |
| Hydrochlorothiazide | 12.5 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]
Selected Package
65862-0308-99Selected1000 TABLET in 1 BOTTLE (65862-308-99)
Other packages for this product(2)
100 TABLET in 1 BOTTLE (65862-308-01)
30 TABLET in 1 BOTTLE (65862-308-30)