Package 0338-9791-40

{"route": ["INTRAVENOUS"], "spl_id": "db478972-6e08-47d1-841c-92b4051a0527", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807633", "1807634", "1807639"], "spl_set_id": ["93aeac13-41de-4452-9f38-d6b4f38ada30"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "40 BAG in 1 CARTON (0338-9791-40)  / 250 mL in 1 BAG (0338-9791-01)", "package_ndc": "0338-9791-40", "marketing_start_date": "20241021"}], "brand_name": "Sodium Chloride", "product_id": "0338-9791_db478972-6e08-47d1-841c-92b4051a0527", "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": "0338-9791", "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": "9 g/1000mL"}], "marketing_category": "UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE", "marketing_start_date": "20241021", "listing_expiration_date": "20261231"}