Package 0990-7904-09

{"route": ["INTRAVENOUS"], "spl_id": "944f8598-ac1a-45af-a5b4-cdc4ea9656ca", "openfda": {"unii": ["660YQ98I10", "451W47IQ8X", "LX22YL083G"], "rxcui": ["615099", "615100", "615107", "615111", "630796", "1863605", "1863607", "1863973"], "spl_set_id": ["d8ee14e9-6733-4813-9f21-2b043a5f7188"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CASE (0990-7904-09)  / 1 BAG in 1 POUCH / 1000 mL in 1 BAG", "package_ndc": "0990-7904-09", "marketing_start_date": "20200201"}], "brand_name": "Potassium Chloride in Dextrose and Sodium Chloride", "product_id": "0990-7904_944f8598-ac1a-45af-a5b4-cdc4ea9656ca", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0990-7904", "generic_name": "DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE", "labeler_name": "ICU Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Dextrose and Sodium Chloride", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "50 g/1000mL"}, {"name": "POTASSIUM CHLORIDE", "strength": "2.98 g/1000mL"}, {"name": "SODIUM CHLORIDE", "strength": "4.5 g/1000mL"}], "application_number": "NDA018362", "marketing_category": "NDA", "marketing_start_date": "20200201", "listing_expiration_date": "20261231"}