Package 0338-0143-03

{"route": ["INTRAVENOUS"], "spl_id": "83a474ed-d005-435f-8ff9-415d4a53ffd6", "openfda": {"unii": ["LX22YL083G", "02F3473H9O", "660YQ98I10", "4J9FJ0HL51", "451W47IQ8X", "TU7HW0W0QT"], "rxcui": ["807396"], "spl_set_id": ["b283a454-0c20-4fbf-92d3-dae1f3cd3cad"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BAG (0338-0143-03)", "package_ndc": "0338-0143-03", "marketing_start_date": "19790202"}], "brand_name": "Dextrose and Electrolyte No. 48", "product_id": "0338-0143_83a474ed-d005-435f-8ff9-415d4a53ffd6", "dosage_form": "INJECTION", "pharm_class": ["Acidifying Activity [MoA]", "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": "0338-0143", "generic_name": "Sodium Lactate, Potassium Chloride, Magnesium Chloride, Monobasic Potassium Phosphate, Sodium Chloride and Dextrose monohydrate", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose and Electrolyte No. 48", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "MAGNESIUM CHLORIDE", "strength": "31 mg/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": "141 mg/100mL"}, {"name": "POTASSIUM PHOSPHATE, MONOBASIC", "strength": "20 mg/100mL"}, {"name": "SODIUM CHLORIDE", "strength": "12 mg/100mL"}, {"name": "SODIUM LACTATE", "strength": "260 mg/100mL"}], "application_number": "NDA017484", "marketing_category": "NDA", "marketing_start_date": "19790202", "listing_expiration_date": "20261231"}