Amlodipine And Benazepril Hydrochloride 71205-0122
Product NDC
71205-0122- Manufacturer
- Proficient Rx Lp
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 5, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA202239
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amlodipine Besylate | 5 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(3)
30 CAPSULE in 1 BOTTLE (71205-122-30)
60 CAPSULE in 1 BOTTLE (71205-122-60)
90 CAPSULE in 1 BOTTLE (71205-122-90)