Package 55154-2348-0

{"route": ["ORAL"], "spl_id": "392096c5-3e3f-47c0-b793-54392f17ccf8", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0055154234900", "0055154234801"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429", "313988"], "spl_set_id": ["2a5bcf50-6d63-463a-915e-a72ea2e5f131"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-2348-0)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "55154-2348-0", "marketing_start_date": "20241204"}], "brand_name": "Furosemide", "product_id": "55154-2348_392096c5-3e3f-47c0-b793-54392f17ccf8", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "55154-2348", "generic_name": "furosemide", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20241204", "listing_expiration_date": "20261231"}