Package 72789-030-30

{"route": ["ORAL"], "spl_id": "3c6c8aa2-377c-0261-e063-6294a90a066b", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0372789030302"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["c24489c3-65e0-44e3-a50a-8bb0672e8821"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-030-30)", "package_ndc": "72789-030-30", "marketing_start_date": "20191205"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-030-60)", "package_ndc": "72789-030-60", "marketing_start_date": "20191205"}], "brand_name": "Furosemide", "product_id": "72789-030_3c6c8aa2-377c-0261-e063-6294a90a066b", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72789-030", "generic_name": "furosemide", "labeler_name": "PD-Rx Pharmaceuticals, 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": "20040326", "listing_expiration_date": "20261231"}