NDC 23155-925 – Amlodipine and Benazepril Hydrochloride
Amlodipine Besylate 10 mg/1; Benazepril Hydrochloride 40 mg/1 · Capsule · Oral
Product NDC23155-925
Product details
- Brand name
- Amlodipine and Benazepril Hydrochloride
- Generic name
- Amlodipine and Benazepril Hydrochloride
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA091431
- Marketed since
- October 15, 2025
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker
Active ingredients
- Amlodipine Besylate 10 mg/1
- Benazepril Hydrochloride 40 mg/1
Uses, dosage, side effects and warnings for Amlodipine and Benazepril Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 23155-925-01 | 100 CAPSULE in 1 BOTTLE (23155-925-01) | Oct 15, 2025 |
| 23155-925-05 | 500 CAPSULE in 1 BOTTLE (23155-925-05) | Oct 15, 2025 |
| 23155-925-10 | 1000 CAPSULE in 1 BOTTLE (23155-925-10) | Oct 15, 2025 |
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