Package 0338-0056-03

{"route": ["INTRAVENOUS"], "spl_id": "44deb447-ac8a-4957-9df5-d9e2f89bc22d", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["730781", "730782"], "spl_set_id": ["181705c7-40e4-4d7d-b9ea-ada99380e7a9"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BAG in 1 CARTON (0338-0056-03)  / 500 mL in 1 BAG", "package_ndc": "0338-0056-03", "marketing_start_date": "19831101"}], "brand_name": "Sodium Chloride", "product_id": "0338-0056_44deb447-ac8a-4957-9df5-d9e2f89bc22d", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0338-0056", "generic_name": "Sodium Chloride", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "5 g/100mL"}], "application_number": "NDA019022", "marketing_category": "NDA", "marketing_start_date": "19831101", "listing_expiration_date": "20261231"}