Lisinopril And Hydrochlorothiazide 68071-4435
Product NDC
68071-4435- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 4, 2003
- Listing Expires
- December 31, 2026
- Application
- ANDA076194
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 12.5 mg/1 |
| Lisinopril | 20 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]
Packaging Options(3)
30 TABLET in 1 BOTTLE (68071-4435-3)
60 TABLET in 1 BOTTLE (68071-4435-6)
90 TABLET in 1 BOTTLE (68071-4435-9)