Package 0990-7905-09

{"route": ["INTRAVENOUS"], "spl_id": "357fc68c-2f4c-4f4c-9e26-a66ff54c59ff", "openfda": {"unii": ["LX22YL083G", "660YQ98I10"], "rxcui": ["309783"], "spl_set_id": ["02d694b5-3600-4d55-bd5c-924abaec5315"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CASE (0990-7905-09)  / 1 BAG in 1 POUCH / 1000 mL in 1 BAG", "package_ndc": "0990-7905-09", "marketing_start_date": "20201120"}], "brand_name": "Potassium Chloride in Dextrose", "product_id": "0990-7905_357fc68c-2f4c-4f4c-9e26-a66ff54c59ff", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0990-7905", "generic_name": "dextrose monohydrate and potassium chloride injection, solution", "labeler_name": "ICU Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": ".149 g/100mL"}], "application_number": "NDA018371", "marketing_category": "NDA", "marketing_start_date": "20201120", "listing_expiration_date": "20261231"}