Amlodipine And Benazepril Hydrochloride 23155-0925
Product NDC
23155-0925- Manufacturer
- Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 15, 2025
- Listing Expires
- December 31, 2027
- Application
- ANDA091431
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amlodipine Besylate | 10 mg/1 |
| Benazepril Hydrochloride | 40 mg/1 |
Drug Class
Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]Calcium Channel Antagonists [MoA]
Packaging Options(3)
100 CAPSULE in 1 BOTTLE (23155-925-01)
500 CAPSULE in 1 BOTTLE (23155-925-05)
1000 CAPSULE in 1 BOTTLE (23155-925-10)