Package 72162-2360-1

{"route": ["ORAL"], "spl_id": "458eb977-b5ff-4cd6-9159-9f9e4f187de9", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898356"], "spl_set_id": ["c870013c-e823-4233-a803-33a74f3610a8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-2360-1)", "package_ndc": "72162-2360-1", "marketing_start_date": "20240628"}], "brand_name": "Amlodipine and Benazepril Hydrochloride", "product_id": "72162-2360_458eb977-b5ff-4cd6-9159-9f9e4f187de9", "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": "72162-2360", "generic_name": "Amlodipine and Benazepril Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and Benazepril Hydrochloride", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA202239", "marketing_category": "ANDA", "marketing_start_date": "20120905", "listing_expiration_date": "20261231"}