Package 43203-852-47

{"route": ["EXTRACORPOREAL"], "spl_id": "49c60185-a86d-44a7-a10e-d0ec57df1fbe", "openfda": {"unii": ["2968PHW8QP", "LX22YL083G", "1Q73Q2JULR"], "spl_set_id": ["b850deac-161f-4bb0-ac7f-bceac2a230c0"], "manufacturer_name": ["Arteriocyte Medical Systems, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 CASE (43203-852-47)  / 1 BAG in 1 POUCH / 50 mL in 1 BAG", "package_ndc": "43203-852-47", "marketing_start_date": "20110511"}], "brand_name": "Anticoagulant Citrate Dextrose A ACD-A", "product_id": "43203-852_49c60185-a86d-44a7-a10e-d0ec57df1fbe", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "43203-852", "generic_name": "Anticoagulant Citrate Dextrose A ACD-A", "labeler_name": "Arteriocyte Medical Systems, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anticoagulant Citrate Dextrose A ACD-A", "active_ingredients": [{"name": "CITRIC ACID MONOHYDRATE", "strength": ".08 g/10mL"}, {"name": "DEXTROSE MONOHYDRATE", "strength": ".245 g/10mL"}, {"name": "SODIUM CITRATE, UNSPECIFIED FORM", "strength": ".22 g/10mL"}], "application_number": "BA110057", "marketing_category": "ANDA", "marketing_start_date": "20110511", "listing_expiration_date": "20261231"}