Package 55111-586-30
Brand: amlodipine besylate and benazepril hydrochloride
Generic: amlodipine besylate and benazepril hydrochloridePackage Facts
Identity
Package NDC
55111-586-30
Digits Only
5511158630
Product NDC
55111-586
Description
30 CAPSULE in 1 BOTTLE (55111-586-30)
Marketing
Marketing Status
Brand
amlodipine besylate and benazepril hydrochloride
Generic
amlodipine besylate and benazepril hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b57e667-c854-2ed1-32f9-b06c6fea1930", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898346", "898359"], "spl_set_id": ["f12f18bb-7ddb-e7dc-4edd-32f4ac212bca"], "manufacturer_name": ["Dr.Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (55111-586-01)", "package_ndc": "55111-586-01", "marketing_start_date": "20110705"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (55111-586-05)", "package_ndc": "55111-586-05", "marketing_start_date": "20110705"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (55111-586-30)", "package_ndc": "55111-586-30", "marketing_start_date": "20110705"}], "brand_name": "Amlodipine Besylate and Benazepril Hydrochloride", "product_id": "55111-586_2b57e667-c854-2ed1-32f9-b06c6fea1930", "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": "55111-586", "generic_name": "Amlodipine Besylate and Benazepril Hydrochloride", "labeler_name": "Dr.Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate and Benazepril Hydrochloride", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA090149", "marketing_category": "ANDA", "marketing_start_date": "20110705", "listing_expiration_date": "20261231"}