Package 70518-3061-3

{"route": ["ORAL"], "spl_id": "3e625d3b-aa68-1274-e063-6294a90acc34", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["3d312ab0-589c-427b-84da-18887244bfc9"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-3061-3)", "package_ndc": "70518-3061-3", "marketing_start_date": "20240426"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE, PLASTIC (70518-3061-5)", "package_ndc": "70518-3061-5", "marketing_start_date": "20240426"}], "brand_name": "Furosemide", "product_id": "70518-3061_3e625d3b-aa68-1274-e063-6294a90acc34", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "70518-3061", "generic_name": "furosemide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20210331", "listing_expiration_date": "20261231"}