anticoagulant sodium citrate
Generic: trisodium citrate dihydrate
Labeler: csl plasma inc.Drug Facts
Product Profile
Brand Name
anticoagulant sodium citrate
Generic Name
trisodium citrate dihydrate
Labeler
csl plasma inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
trisodium citrate dihydrate 40 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
81839-782
Product ID
81839-782_2f9d0600-c8af-4701-aadb-ee29592f7a12
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
BA125750
Listing Expiration
2026-12-31
Marketing Start
2022-07-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
81839782
Hyphenated Format
81839-782
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
anticoagulant sodium citrate (source: ndc)
Generic Name
trisodium citrate dihydrate (source: ndc)
Application Number
BA125750 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/mL
Packaging
- 30 BAG in 1 CARTON (81839-782-02) / 250 mL in 1 BAG (81839-782-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}