Amlodipine and Benazepril Hydrochloride
- Product NDC
- 50090-7361
- 11-digit product format
- 500907361
- Labeler code
- 50090
- Product ID
- 50090-7361_90815557-bb3d-4587-b552-b255bf040c14
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine and Benazepril Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202239
- Marketing category
- ANDA
- Marketing start
- 2012-09-05
- Substance
- AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
- Active strength
- 10; 20 mg/1; mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 864V2Q084H | AMLODIPINE BESYLATE | 111470-99-6 | AMLODIPINE BESYLATE |
| N1SN99T69T | BENAZEPRIL HYDROCHLORIDE | 86541-74-4 | BENAZEPRIL HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7361-0 | 50090736100 | 30 CAPSULE in 1 BOTTLE (50090-7361-0) | 30 capsule | 2024-10-17 | No | No | Historical |
| 50090-7361-1 | 50090736101 | 90 CAPSULE in 1 BOTTLE (50090-7361-1) | 90 capsule | 2024-10-17 | No | No | Historical |