Package 72603-298-02

{"route": ["ORAL"], "spl_id": "3aa9066b-354b-4f6b-87b9-2752a3a51f6b", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0372603298017", "0372603297010", "0372603299014"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["6b92460e-48ba-44bb-9b61-5e65e5fd82cd"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["NorthStar Rx, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-298-01)", "package_ndc": "72603-298-01", "marketing_start_date": "20250901"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72603-298-02)", "package_ndc": "72603-298-02", "marketing_start_date": "20250901"}], "brand_name": "bumetanide", "product_id": "72603-298_3aa9066b-354b-4f6b-87b9-2752a3a51f6b", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72603-298", "generic_name": "bumetanide", "labeler_name": "NorthStar Rx, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "ANDA074225", "marketing_category": "ANDA", "marketing_start_date": "20250901", "listing_expiration_date": "20261231"}