Package 72789-432-90

{"route": ["ORAL"], "spl_id": "383ed601-2a4c-7fd9-e063-6394a90a2bee", "openfda": {"upc": ["0372789432908"], "unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898353"], "spl_set_id": ["ff807933-7433-4f8c-9d09-02a57e51d0fc"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (72789-432-90)", "package_ndc": "72789-432-90", "marketing_start_date": "20240926"}], "brand_name": "Amlodipine Besylate and Benazepril Hydrochloride", "product_id": "72789-432_383ed601-2a4c-7fd9-e063-6394a90a2bee", "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": "72789-432", "generic_name": "Amlodipine Besylate and Benazepril Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate and Benazepril Hydrochloride", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078466", "marketing_category": "ANDA", "marketing_start_date": "20100205", "listing_expiration_date": "20261231"}