Lisinopril And Hydrochlorothiazide 00591-0861
Product NDC
00591-0861- Manufacturer
- Actavis Pharma, 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(2)
100 TABLET in 1 BOTTLE, PLASTIC (0591-0861-01)
500 TABLET in 1 BOTTLE, PLASTIC (0591-0861-05)