Package 23731-6051-1

Brand: anticoagulant citrate dextrose a

Generic: anhydrous citric acid, dextrose monohydrate, and trisodium citrate dihydrate
NDC Package

Package Facts

Identity

Package NDC 23731-6051-1
Digits Only 2373160511
Product NDC 23731-6051
Product ID 23731-6051_9a133b17-0377-431f-b839-3e090fdabd78
Description

10 VIAL, SINGLE-USE in 1 CASE (23731-6051-1) / 30 mL in 1 VIAL, SINGLE-USE (23731-6051-3)

Marketing

Marketing Status
Marketed Since 2003-08-26
Brand anticoagulant citrate dextrose a
Generic anhydrous citric acid, dextrose monohydrate, and trisodium citrate dihydrate
Sample Package No

Linked Drug Pages (1)

Anticoagulant Citrate Dextrose A ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["EXTRACORPOREAL"], "spl_id": "9a133b17-0377-431f-b839-3e090fdabd78", "openfda": {"nui": ["N0000175833", "N0000175835", "N0000175980", "N0000008556", "N0000175089"], "unii": ["XF417D3PSL", "LX22YL083G", "B22547B95K"], "spl_set_id": ["5bcd261e-ebba-4ecb-af22-e5aaeb04499b"], "pharm_class_pe": ["Decreased Coagulation Factor Activity [PE]"], "pharm_class_epc": ["Calculi Dissolution Agent [EPC]", "Anti-coagulant [EPC]"], "pharm_class_moa": ["Acidifying Activity [MoA]", "Calcium Chelating Activity [MoA]"], "manufacturer_name": ["Citra Labs LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CASE (23731-6051-1)  / 30 mL in 1 VIAL, SINGLE-USE (23731-6051-3)", "package_ndc": "23731-6051-1", "marketing_start_date": "20030826"}, {"sample": false, "description": "25 VIAL, SINGLE-USE in 1 CASE (23731-6051-2)  / 30 mL in 1 VIAL, SINGLE-USE (23731-6051-3)", "package_ndc": "23731-6051-2", "marketing_start_date": "20030826"}, {"sample": false, "description": "30 mL in 1 VIAL, SINGLE-USE (23731-6051-3)", "package_ndc": "23731-6051-3", "marketing_start_date": "20030826"}], "brand_name": "Anticoagulant Citrate Dextrose A", "product_id": "23731-6051_9a133b17-0377-431f-b839-3e090fdabd78", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "23731-6051", "generic_name": "Anhydrous Citric Acid, Dextrose Monohydrate, and Trisodium Citrate Dihydrate", "labeler_name": "Citra Labs LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anticoagulant Citrate Dextrose A", "active_ingredients": [{"name": "ANHYDROUS CITRIC ACID", "strength": ".073 g/10mL"}, {"name": "DEXTROSE MONOHYDRATE", "strength": ".245 g/10mL"}, {"name": "TRISODIUM CITRATE DIHYDRATE", "strength": ".22 g/10mL"}], "application_number": "BN020037", "marketing_category": "NDA", "marketing_start_date": "20030826", "listing_expiration_date": "20261231"}