Package 0990-7075-14

{"route": ["INTRAVENOUS"], "spl_id": "88bcbbe4-9ebf-4491-874a-c4c4c7f1f90d", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312507", "1860239", "1860241", "1860463", "1860466"], "spl_set_id": ["eb56a807-ea94-4edb-9811-a04b19568468"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 POUCH in 1 CASE (0990-7075-14)  / 1 BAG in 1 POUCH / 50 mL in 1 BAG", "package_ndc": "0990-7075-14", "marketing_start_date": "20190401"}, {"sample": false, "description": "24 POUCH in 1 CASE (0990-7075-26)  / 1 BAG in 1 POUCH / 100 mL in 1 BAG", "package_ndc": "0990-7075-26", "marketing_start_date": "20190401"}], "brand_name": "Potassium Chloride", "product_id": "0990-7075_88bcbbe4-9ebf-4491-874a-c4c4c7f1f90d", "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": "0990-7075", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "ICU Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "200 meq/1000mL"}], "application_number": "NDA020161", "marketing_category": "NDA", "marketing_start_date": "20190401", "listing_expiration_date": "20261231"}