Prescription drug · NDA
Lotrel NDC 0078-0379
amlodipine besylate and benazepril hydrochloride · Amlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1 · Capsule · Oral · Novartis Pharmaceuticals Corporation
NDC codes
FDA NDC DirectoryProduct NDC (as listed)0078-0379Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00078-0379Add the package segment from the table below.
Product information
- Brand name (proprietary)
- Lotrel
- Generic name (nonproprietary)
- amlodipine besylate and benazepril hydrochloride
- Active ingredients
- Amlodipine besylate — 10 mg/1Benazepril hydrochloride — 40 mg/1
- Dosage form
- Capsule
- Route
- Oral
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 020364
- Marketing start
- Marketing end
- Other FDA classes
- Angiotensin-converting Enzyme Inhibitors (Mechanism)Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)Dihydropyridines (Chemical structure)
- Identifiers
- Product ID 0078-0379_b9db75d9-9d1e-4b2d-9876-5f5520feaeccSPL ID b9db75d9-9d1e-4b2d-9876-5f5520feaeccSPL set ID 94ae6054-b7ae-4212-a567-4f803af8f2c7RxCUI 898342, 898344, 898346, 898348, 898353, 898355, 898356, 898358UNII 864V2Q084H, N1SN99T69T
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
Product label
Label details couldn’t be retrieved right now. Open the label on DailyMed.