Package 0990-9257-39

{"route": ["INTRAVENOUS"], "spl_id": "75d665b8-1e91-436f-86f6-ca8d284ab438", "openfda": {"unii": ["660YQ98I10", "451W47IQ8X"], "rxcui": ["403890"], "spl_set_id": ["243fe8fc-996a-4855-8daf-069628e547c4"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CASE (0990-9257-39)  / 1 BAG in 1 POUCH / 1000 mL in 1 BAG", "package_ndc": "0990-9257-39", "marketing_start_date": "20200301"}], "brand_name": "Potassium Chloride in Sodium Chloride", "product_id": "0990-9257_75d665b8-1e91-436f-86f6-ca8d284ab438", "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": "0990-9257", "generic_name": "SODIUM CHLORIDE and POTASSIUM CHLORIDE", "labeler_name": "ICU Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Sodium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.49 g/1000mL"}, {"name": "SODIUM CHLORIDE", "strength": "4.5 g/1000mL"}], "application_number": "ANDA078446", "marketing_category": "ANDA", "marketing_start_date": "20200101", "listing_expiration_date": "20261231"}