Lisinopril And Hydrochlorothiazide 68180-0519
Product NDC
68180-0519- Manufacturer
- Lupin Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 4, 2006
- Listing Expires
- December 31, 2026
- Application
- ANDA077912
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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)
100 TABLET in 1 BOTTLE (68180-519-01)
500 TABLET in 1 BOTTLE (68180-519-02)
5000 TABLET in 1 POUCH (68180-519-30)