Package 70518-0251-2

{"route": ["ORAL"], "spl_id": "47e58bf6-e13d-346e-e063-6294a90a690c", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["916de29e-228c-4dfc-bcee-ad9a641316bd"], "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": "90 TABLET in 1 BOTTLE, PLASTIC (70518-0251-1)", "package_ndc": "70518-0251-1", "marketing_start_date": "20170317"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70518-0251-2)", "package_ndc": "70518-0251-2", "marketing_start_date": "20170421"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0251-3)", "package_ndc": "70518-0251-3", "marketing_start_date": "20180410"}], "brand_name": "Furosemide", "product_id": "70518-0251_47e58bf6-e13d-346e-e063-6294a90a690c", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "70518-0251", "generic_name": "Furosemide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20170222", "listing_expiration_date": "20271231"}