Package 17271-734-07

{"route": ["INTRAVENOUS"], "spl_id": "cfe5e2b2-fe4e-4fa2-9dee-3197ac1de46d", "openfda": {"unii": ["LX22YL083G", "451W47IQ8X"], "rxcui": ["1795250", "1795252", "1795254"], "spl_set_id": ["d3f90d2f-4536-4d32-800b-7a798f8a35db"], "manufacturer_name": ["BECTON DICKINSON AND COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BAG in 1 CASE (17271-734-05)  / 250 mL in 1 BAG", "package_ndc": "17271-734-05", "marketing_start_date": "20250515"}, {"sample": false, "description": "20 BAG in 1 CASE (17271-734-06)  / 500 mL in 1 BAG", "package_ndc": "17271-734-06", "marketing_start_date": "20250515"}, {"sample": false, "description": "10 BAG in 1 CASE (17271-734-07)  / 1000 mL in 1 BAG", "package_ndc": "17271-734-07", "marketing_start_date": "20250515"}], "brand_name": "Dextrose and Sodium Chloride", "product_id": "17271-734_cfe5e2b2-fe4e-4fa2-9dee-3197ac1de46d", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "17271-734", "generic_name": "DEXTROSE MONOHYDRATE and SODIUM CHLORIDE", "labeler_name": "BECTON DICKINSON AND COMPANY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose and Sodium Chloride", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "SODIUM CHLORIDE", "strength": ".45 g/100mL"}], "application_number": "ANDA211276", "marketing_category": "ANDA", "marketing_start_date": "20201026", "listing_expiration_date": "20261231"}