Package 57237-147-01

Brand: amlodipine and benazepril hydrochloride

Generic: amlodipine and benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 57237-147-01
Digits Only 5723714701
Product NDC 57237-147
Description

100 CAPSULE in 1 BOTTLE (57237-147-01)

Marketing

Marketing Status
Marketed Since 2012-09-05
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": "a4aff76f-e9a9-4300-b42c-616d8ca55d5d", "openfda": {"upc": ["0357237143018", "0357237142011", "0357237146019", "0357237147016", "0357237145012", "0357237144015"], "unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898342", "898346", "898350", "898353", "898356", "898359"], "spl_set_id": ["03b175fc-d430-490d-b7ac-9f7a2cb1dd8b"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (57237-147-01)", "package_ndc": "57237-147-01", "marketing_start_date": "20120905"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (57237-147-05)", "package_ndc": "57237-147-05", "marketing_start_date": "20120905"}], "brand_name": "Amlodipine and Benazepril Hydrochloride", "product_id": "57237-147_a4aff76f-e9a9-4300-b42c-616d8ca55d5d", "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": "57237-147", "generic_name": "Amlodipine and Benazepril Hydrochloride", "labeler_name": "Rising Pharma Holdings, 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": "ANDA202239", "marketing_category": "ANDA", "marketing_start_date": "20120905", "listing_expiration_date": "20261231"}