Package 0338-0683-04

{"route": ["INTRAVENOUS"], "spl_id": "b312752a-f970-43c1-96de-eccf5a461e88", "openfda": {"unii": ["LX22YL083G", "660YQ98I10"], "rxcui": ["309783"], "spl_set_id": ["45de5402-5e61-4bbd-8bbc-5e3392c9920e"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BAG (0338-0683-04)", "package_ndc": "0338-0683-04", "marketing_start_date": "19790201"}], "brand_name": "Potassium Chloride in Dextrose", "product_id": "0338-0683_b312752a-f970-43c1-96de-eccf5a461e88", "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": "0338-0683", "generic_name": "Potassium Chloride and Dextrose Monohydrate", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": "150 mg/100mL"}], "application_number": "NDA017634", "marketing_category": "NDA", "marketing_start_date": "19790201", "listing_expiration_date": "20261231"}