Package 70518-4386-0

{"route": ["ORAL"], "spl_id": "3955ccba-7a60-dca6-e063-6294a90ac88d", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898356"], "spl_set_id": ["dc206611-5188-40a6-b025-61db41f68a5a"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-4386-0)", "package_ndc": "70518-4386-0", "marketing_start_date": "20250706"}], "brand_name": "Amlodipine Besylate and Benazepril Hydrochloride", "product_id": "70518-4386_3955ccba-7a60-dca6-e063-6294a90ac88d", "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": "70518-4386", "generic_name": "Amlodipine Besylate and Benazepril Hydrochloride", "labeler_name": "REMEDYREPACK 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": "20 mg/1"}], "application_number": "ANDA078466", "marketing_category": "ANDA", "marketing_start_date": "20250706", "listing_expiration_date": "20261231"}