Amlodipine and Benazepril Hydrochloride
Amlodipine and Benazepril Hydrochloride is listed in the FDA National Drug Code directory with 46 NDC codes, marketed under brand name including Amlodipine and Benazepril Hydrochloride. Available dosage form: capsule.
Drug Details
- Generic Name
- Amlodipine and Benazepril Hydrochloride
- Brand Names
- Amlodipine and Benazepril Hydrochloride
- Application Number
- ANDA091431
- Sponsor
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- NDC Codes
- 46
- Dosage Forms
- CAPSULE
- Routes
- ORAL
- Active Ingredients
- AMLODIPINE BESYLATE, BENAZEPRIL HYDROCHLORIDE
Indications and Usage
1 INDICATIONS AND USAGE Amlodipine and benazepril hydrochloride capsules are a combination capsule of amlodipine, a dihydropyridine calcium channel blocker (DHP CCB) and benazepril, an angiotensin-converting enzyme (ACE) inhibitor. Amlodipine and benazepril hydrochloride capsules are indicated for the treatment of hypertension in patients not adequately controlled on monotherapy with either agent. (1) 1.1 Hypertension Amlodipine and benazepril hydrochloride capsules are indicated for the treatment of hypertension in patients not adequately controlled on monotherapy with either agent.