NDC 50090-7361 – Amlodipine and Benazepril Hydrochloride
Amlodipine Besylate 10 mg/1; Benazepril Hydrochloride 20 mg/1 · Capsule · Oral
Product NDC50090-7361
Product details
- Brand name
- Amlodipine and Benazepril Hydrochloride
- Generic name
- Amlodipine and Benazepril Hydrochloride
- Labeler
- A-S Medication Solutions
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA202239
- Marketed since
- September 5, 2012
- Listing expires
- December 31, 2026
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 50090-7361-0 | 30 CAPSULE in 1 BOTTLE (50090-7361-0) | Oct 17, 2024 |
| 50090-7361-1 | 90 CAPSULE in 1 BOTTLE (50090-7361-1) | Oct 17, 2024 |
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