Lisinopril 68788-6920
Product NDC
68788-6920- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 6, 2017
- Listing Expires
- December 31, 2027
- Application
- ANDA076164
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lisinopril | 20 mg/1 |
Drug Class
Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]
Packaging Options(4)
100 TABLET in 1 BOTTLE (68788-6920-1)
30 TABLET in 1 BOTTLE (68788-6920-3)
60 TABLET in 1 BOTTLE (68788-6920-6)
90 TABLET in 1 BOTTLE (68788-6920-9)