Package 0338-0671-04
Brand: potassium chloride in dextrose and sodium chloride
Generic: potassium chloride, dextrose monohydrate and sodium chloridePackage Facts
Identity
Package NDC
0338-0671-04
Digits Only
0338067104
Product NDC
0338-0671
Description
1000 mL in 1 BAG (0338-0671-04)
Marketing
Marketing Status
Brand
potassium chloride in dextrose and sodium chloride
Generic
potassium chloride, dextrose monohydrate and sodium chloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "34c74d23-f49a-4e1c-9ffe-9a200d0fffe7", "openfda": {"unii": ["660YQ98I10", "451W47IQ8X", "LX22YL083G"], "rxcui": ["615099", "615100", "615107", "615111", "630796", "1863605", "1863607", "1863973", "1863975", "1863988"], "spl_set_id": ["c553fed1-3de5-4826-8eff-633b5923bf0b"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BAG (0338-0671-04)", "package_ndc": "0338-0671-04", "marketing_start_date": "19790202"}], "brand_name": "Potassium Chloride in Dextrose and Sodium Chloride", "product_id": "0338-0671_34c74d23-f49a-4e1c-9ffe-9a200d0fffe7", "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": "0338-0671", "generic_name": "Potassium Chloride, Dextrose Monohydrate and Sodium Chloride", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Dextrose and Sodium Chloride", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": "150 mg/100mL"}, {"name": "SODIUM CHLORIDE", "strength": "450 mg/100mL"}], "application_number": "NDA018008", "marketing_category": "NDA", "marketing_start_date": "19790202", "listing_expiration_date": "20261231"}