Package 72189-260-90

{"route": ["ORAL"], "spl_id": "2be94c25-4a48-39f0-e063-6294a90ab40c", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["308136", "898342"], "spl_set_id": ["b8b9a3cd-c4e7-dfeb-e053-2a95a90aa719"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72189-260-90)", "package_ndc": "72189-260-90", "marketing_start_date": "20210810"}], "brand_name": "AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE", "product_id": "72189-260_2be94c25-4a48-39f0-e063-6294a90ab40c", "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": "72189-260", "generic_name": "AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE", "labeler_name": "DIRECT RX", "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": "20 mg/1"}], "application_number": "ANDA202239", "marketing_category": "ANDA", "marketing_start_date": "20210810", "listing_expiration_date": "20261231"}