Benazepril Hydrochloride 51655-0066
Product NDC
51655-0066- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 4, 2016
- Listing Expires
- December 31, 2027
- Application
- ANDA076118
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Benazepril Hydrochloride | 20 mg/1 |
Drug Class
Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]Decreased Blood Pressure [PE]
Packaging Options(2)
90 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-066-26)
30 TABLET, COATED in 1 BOTTLE, DISPENSING (51655-066-52)