NDC 84677-012 – Amlodipine and Benazepril Hydrochloride
Amlodipine Besylate 10 mg/1; Benazepril Hydrochloride 20 mg/1 · Capsule · Oral
Product NDC84677-012
Product details
- Brand name
- Amlodipine and Benazepril Hydrochloride
- Generic name
- Amlodipine and Benazepril Hydrochloride
- Labeler
- Golden State Medical Supply, Inc.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA091431
- Marketed since
- December 30, 2013
- 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 20 mg/1
Uses, dosage, side effects and warnings for Amlodipine and Benazepril Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 84677-012-01 | 100 CAPSULE in 1 BOTTLE (84677-012-01) | Jul 27, 2026 |
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