Amlodipine Besylate And Benazepril Hydrochloride 82868-0041
Product NDC
82868-0041- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 19, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA077183
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amlodipine Besylate | 10 mg/1 |
| Benazepril Hydrochloride | 20 mg/1 |
Drug Class
Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]Calcium Channel Antagonists [MoA]
Packaging Options(1)
90 CAPSULE in 1 BOTTLE, PLASTIC (82868-041-90)