Package 63323-874-10

{"route": ["INTRAVENOUS"], "spl_id": "246065b3-688f-43b6-b847-9ba16ac639d4", "openfda": {"unii": ["LX22YL083G", "451W47IQ8X"], "rxcui": ["1795470"], "spl_set_id": ["b825c9c4-f2fb-4a4a-9d8c-fb020ad07e93"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BAG in 1 CASE (63323-874-10)  / 1000 mL in 1 BAG", "package_ndc": "63323-874-10", "marketing_start_date": "20210301"}], "brand_name": "DEXTROSE AND SODIUM CHLORIDE", "product_id": "63323-874_246065b3-688f-43b6-b847-9ba16ac639d4", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "63323-874", "generic_name": "DEXTROSE MONOHYDRATE, SODIUM CHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXTROSE AND SODIUM CHLORIDE", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "2.5 g/100mL"}, {"name": "SODIUM CHLORIDE", "strength": ".45 g/100mL"}], "application_number": "ANDA211190", "marketing_category": "ANDA", "marketing_start_date": "20210301", "listing_expiration_date": "20261231"}