Package 81839-782-02

Brand: anticoagulant sodium citrate

Generic: trisodium citrate dihydrate
NDC Package

Package Facts

Identity

Package NDC 81839-782-02
Digits Only 8183978202
Product NDC 81839-782
Product ID 81839-782_2f9d0600-c8af-4701-aadb-ee29592f7a12
Description

30 BAG in 1 CARTON (81839-782-02) / 250 mL in 1 BAG (81839-782-01)

Marketing

Marketing Status
Marketed Since 2022-07-01
Brand anticoagulant sodium citrate
Generic trisodium citrate dihydrate
Sample Package No

Linked Drug Pages (1)

Anticoagulant Sodium Citrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "2f9d0600-c8af-4701-aadb-ee29592f7a12", "openfda": {"unii": ["B22547B95K"], "spl_set_id": ["1798dd96-5ae7-4a8b-b433-24ca9b38d863"], "manufacturer_name": ["CSL Plasma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BAG in 1 CARTON (81839-782-02)  / 250 mL in 1 BAG (81839-782-01)", "package_ndc": "81839-782-02", "marketing_start_date": "20220701"}], "brand_name": "Anticoagulant Sodium Citrate", "product_id": "81839-782_2f9d0600-c8af-4701-aadb-ee29592f7a12", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "81839-782", "generic_name": "Trisodium Citrate Dihydrate", "labeler_name": "CSL Plasma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anticoagulant Sodium Citrate", "active_ingredients": [{"name": "TRISODIUM CITRATE DIHYDRATE", "strength": "40 mg/mL"}], "application_number": "BA125750", "marketing_category": "ANDA", "marketing_start_date": "20220701", "listing_expiration_date": "20261231"}