Package 63323-099-63

{"route": ["INTRAVENOUS"], "spl_id": "f5197532-af45-42c9-919b-30d00276650e", "openfda": {"upc": ["0363323099039"], "unii": ["451W47IQ8X"], "rxcui": ["313016"], "spl_set_id": ["b6e33138-841a-471f-a934-c4086cbc23f6"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, PLASTIC in 1 TRAY (63323-099-63)  / 200 mL in 1 VIAL, PLASTIC (63323-099-03)", "package_ndc": "63323-099-63", "marketing_start_date": "20230711"}], "brand_name": "Sodium Chloride", "product_id": "63323-099_f5197532-af45-42c9-919b-30d00276650e", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "63323-099", "generic_name": "Sodium Chloride", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "4 meq/mL"}], "application_number": "ANDA217796", "marketing_category": "ANDA", "marketing_start_date": "20230711", "listing_expiration_date": "20261231"}