Package 70518-4388-0

{"route": ["ORAL"], "spl_id": "39566a39-b9f2-4b9c-e063-6394a90aff7a", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898359"], "spl_set_id": ["2542895b-c8f8-4f21-9e12-f5a7fe17f905"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-4388-0)", "package_ndc": "70518-4388-0", "marketing_start_date": "20250706"}], "brand_name": "Amlodipine Besylate and Benazepril Hydrochloride", "product_id": "70518-4388_39566a39-b9f2-4b9c-e063-6394a90aff7a", "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": "70518-4388", "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": "40 mg/1"}], "application_number": "ANDA090149", "marketing_category": "ANDA", "marketing_start_date": "20250706", "listing_expiration_date": "20261231"}