Package 0990-7925-09

{"route": ["INTRAVENOUS"], "spl_id": "391a9854-64db-4da4-b8a5-a230001aa81c", "openfda": {"unii": ["451W47IQ8X", "LX22YL083G"], "rxcui": ["1794902", "1794904", "1794905", "1795149", "1795150", "1795250", "1795252", "1795254", "1795344", "1795346"], "spl_set_id": ["4555b1bf-6d97-4798-a63d-6d34291c85ce"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 POUCH in 1 CASE (0990-7925-03)  / 1 BAG in 1 POUCH / 500 mL in 1 BAG", "package_ndc": "0990-7925-03", "marketing_start_date": "20191125"}, {"sample": false, "description": "12 POUCH in 1 CASE (0990-7925-09)  / 1 BAG in 1 POUCH / 1000 mL in 1 BAG", "package_ndc": "0990-7925-09", "marketing_start_date": "20191201"}], "brand_name": "Dextrose and Sodium Chloride", "product_id": "0990-7925_391a9854-64db-4da4-b8a5-a230001aa81c", "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": "0990-7925", "generic_name": "DEXTROSE MONOHYDRATE and SODIUM CHLORIDE", "labeler_name": "ICU Medical Inc.", "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": ".3 g/100mL"}], "application_number": "NDA017799", "marketing_category": "NDA", "marketing_start_date": "20190901", "listing_expiration_date": "20261231"}