NDC 68001-132 – Amlodipine Besylate and Benazepril Hydrochloride
Amlodipine Besylate 2.5 mg/1; Benazepril Hydrochloride 10 mg/1 · Capsule · Oral
Product NDC68001-132
Product details
- Brand name
- Amlodipine Besylate and Benazepril Hydrochloride
- Generic name
- Amlodipine Besylate and Benazepril Hydrochloride
- Labeler
- BluePoint Laboratories
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA078466
- Marketed since
- July 16, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker
Active ingredients
- Amlodipine Besylate 2.5 mg/1
- Benazepril Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Amlodipine Besylate and Benazepril Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68001-132-00 | 100 CAPSULE in 1 BOTTLE (68001-132-00) | Jul 16, 2015 |
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