Package 23155-925-01
Brand: amlodipine and benazepril hydrochloride
Generic: amlodipine and benazepril hydrochloridePackage Facts
Identity
Package NDC
23155-925-01
Digits Only
2315592501
Product NDC
23155-925
Description
100 CAPSULE in 1 BOTTLE (23155-925-01)
Marketing
Marketing Status
Brand
amlodipine and benazepril hydrochloride
Generic
amlodipine and benazepril hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e2f5c585-ebd4-430f-bbc7-37ba524bda85", "openfda": {"upc": ["0323155925012", "0323155920109", "0323155922059", "0323155925104", "0323155920017", "0323155922103", "0323155925050", "0323155920055", "0323155922011"], "unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898346", "898350", "898356"], "spl_set_id": ["27b0c628-820a-48bf-a411-86c0ebd4cc8d"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (23155-925-01)", "package_ndc": "23155-925-01", "marketing_start_date": "20251015"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (23155-925-05)", "package_ndc": "23155-925-05", "marketing_start_date": "20251015"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (23155-925-10)", "package_ndc": "23155-925-10", "marketing_start_date": "20251015"}], "brand_name": "Amlodipine and Benazepril Hydrochloride", "product_id": "23155-925_e2f5c585-ebd4-430f-bbc7-37ba524bda85", "dosage_form": "CAPSULE", "pharm_class": ["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]"], "product_ndc": "23155-925", "generic_name": "Amlodipine and Benazepril Hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and Benazepril Hydrochloride", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA091431", "marketing_category": "ANDA", "marketing_start_date": "20251015", "listing_expiration_date": "20271231"}