Quinapril Hcl And Hydrochlorothiazide 43386-0712
Product NDC
43386-0712- Manufacturer
- Lupin Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 15, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA076374
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 25 mg/1 |
| Quinapril Hydrochloride | 20 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]
Packaging Options(2)
500 TABLET in 1 BOTTLE (43386-712-05)
90 TABLET in 1 BOTTLE (43386-712-09)