Package 0338-0691-04

{"route": ["INTRAVENOUS"], "spl_id": "0770d1c7-920a-4569-9e1d-de264bea58b1", "openfda": {"unii": ["660YQ98I10", "451W47IQ8X"], "rxcui": ["237367", "403890", "637551"], "spl_set_id": ["becc7410-0a25-49f5-b0c3-240078479dc8"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 BAG in 1 CARTON (0338-0691-04)  / 1000 mL in 1 BAG", "package_ndc": "0338-0691-04", "marketing_start_date": "19790202"}], "brand_name": "Potassium Chloride in Sodium Chloride", "product_id": "0338-0691_0770d1c7-920a-4569-9e1d-de264bea58b1", "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": "0338-0691", "generic_name": "Potassium Chloride and Sodium Chloride", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Sodium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "150 mg/100mL"}, {"name": "SODIUM CHLORIDE", "strength": "900 mg/100mL"}], "application_number": "NDA017648", "marketing_category": "NDA", "marketing_start_date": "19790202", "listing_expiration_date": "20261231"}