Package 65219-146-10

{"route": ["INTRAVENOUS"], "spl_id": "93737cd2-f9e0-41e1-9263-2c4ff516395a", "openfda": {"unii": ["660YQ98I10", "451W47IQ8X", "LX22YL083G"], "rxcui": ["615099", "615100", "630796", "1863605", "1863607"], "spl_set_id": ["fe5b5182-c859-4c74-b2e0-467be5b2e329"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BAG in 1 CASE (65219-146-10)  / 1000 mL in 1 BAG (65219-146-06)", "package_ndc": "65219-146-10", "marketing_start_date": "20220826"}], "brand_name": "Potassium Chloride in Dextrose and Sodium Chloride", "product_id": "65219-146_93737cd2-f9e0-41e1-9263-2c4ff516395a", "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": "65219-146", "generic_name": "DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "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": "2.24 g/1000mL"}, {"name": "SODIUM CHLORIDE", "strength": "4.5 g/1000mL"}], "application_number": "ANDA213523", "marketing_category": "ANDA", "marketing_start_date": "20220826", "listing_expiration_date": "20261231"}