Package 60687-384-65

{"route": ["ORAL"], "spl_id": "21374d66-9881-6023-e063-6394a90a39d2", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197418", "197419"], "spl_set_id": ["5e9633e4-151b-4f40-885e-8f364f6f2d18"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-384-01)  / 1 TABLET in 1 BLISTER PACK (60687-384-11)", "package_ndc": "60687-384-01", "marketing_start_date": "20200713"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (60687-384-65)  / 1 TABLET in 1 BLISTER PACK (60687-384-11)", "package_ndc": "60687-384-65", "marketing_start_date": "20230605"}], "brand_name": "Bumetanide", "product_id": "60687-384_21374d66-9881-6023-e063-6394a90a39d2", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "60687-384", "generic_name": "Bumetanide", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "NDA018225", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20180802", "listing_expiration_date": "20261231"}