Benazepril Hydrochloride 53746-0751
Product NDC
53746-0751- Manufacturer
- Amneal Pharmaceuticals Of New York Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 26, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA076820
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Benazepril Hydrochloride | 5 mg/1 |
Drug Class
Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]Decreased Blood Pressure [PE]
Packaging Options(2)
100 TABLET in 1 BOTTLE (53746-751-01)
500 TABLET in 1 BOTTLE (53746-751-05)