Benazepril Hydrochloride 70518-2125
Product NDC
70518-2125- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 31, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA076118
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Benazepril Hydrochloride | 40 mg/1 |
Drug Class
Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]Decreased Blood Pressure [PE]
Packaging Options(1)
90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2125-0)