Package 0338-0089-03

{"route": ["INTRAVENOUS"], "spl_id": "b4404498-6ab7-4c25-a5a2-5377a6dfecca", "openfda": {"unii": ["451W47IQ8X", "LX22YL083G"], "rxcui": ["1794881", "1794886", "1794887", "1795250", "1795252", "1795344", "1795346", "1795470"], "spl_set_id": ["dcbf1907-1841-4afc-ab5d-a9893a2d7256"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BAG in 1 CARTON (0338-0089-03)  / 500 mL in 1 BAG", "package_ndc": "0338-0089-03", "marketing_start_date": "19701209"}, {"sample": false, "description": "14 BAG in 1 CARTON (0338-0089-04)  / 1000 mL in 1 BAG", "package_ndc": "0338-0089-04", "marketing_start_date": "19701209"}], "brand_name": "Dextrose and Sodium Chloride", "product_id": "0338-0089_b4404498-6ab7-4c25-a5a2-5377a6dfecca", "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": "0338-0089", "generic_name": "Dextrose and Sodium Chloride", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose and Sodium Chloride", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "SODIUM CHLORIDE", "strength": "900 mg/100mL"}], "application_number": "NDA016678", "marketing_category": "NDA", "marketing_start_date": "19701209", "listing_expiration_date": "20261231"}