Package 0264-7645-00

{"route": ["INTRAVENOUS"], "spl_id": "ed62bbc9-60b1-41c1-ae42-846cb79daa11", "openfda": {"unii": ["660YQ98I10", "451W47IQ8X", "IY9XDZ35W2"], "rxcui": ["615099", "615100", "615107", "630796", "1863605", "1863973", "1863988", "1866190"], "spl_set_id": ["59ccc717-c374-41c0-be58-9647df881160"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 CONTAINER in 1 CASE (0264-7645-00)  / 1000 mL in 1 CONTAINER", "package_ndc": "0264-7645-00", "marketing_start_date": "19880217"}], "brand_name": "Potassium Chloride in Dextrose and Sodium Chloride", "product_id": "0264-7645_ed62bbc9-60b1-41c1-ae42-846cb79daa11", "dosage_form": "INJECTION", "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": "0264-7645", "generic_name": "DEXTROSE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Dextrose and Sodium Chloride", "active_ingredients": [{"name": "DEXTROSE, UNSPECIFIED FORM", "strength": "5 g/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": ".15 g/100mL"}, {"name": "SODIUM CHLORIDE", "strength": ".2 g/100mL"}], "application_number": "NDA019630", "marketing_category": "NDA", "marketing_start_date": "19880217", "listing_expiration_date": "20261231"}