anticoagulant citrate dextrose a

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

Labeler: citra labs llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name anticoagulant citrate dextrose a
Generic Name anhydrous citric acid, dextrose monohydrate, and trisodium citrate dihydrate
Labeler citra labs llc
Dosage Form SOLUTION
Routes
EXTRACORPOREAL
Active Ingredients

anhydrous citric acid .073 g/10mL, dextrose monohydrate .245 g/10mL, trisodium citrate dihydrate .22 g/10mL

Manufacturer
Citra Labs LLC

Identifiers & Regulatory

Product NDC 23731-6051
Product ID 23731-6051_9a133b17-0377-431f-b839-3e090fdabd78
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number BN020037
Listing Expiration 2026-12-31
Marketing Start 2003-08-26

Pharmacologic Class

Established (EPC)
calculi dissolution agent [epc] anti-coagulant [epc]
Mechanism of Action
acidifying activity [moa] calcium chelating activity [moa]
Physiologic Effect
decreased coagulation factor activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 237316051
Hyphenated Format 23731-6051

Supplemental Identifiers

UNII
XF417D3PSL LX22YL083G B22547B95K
NUI
N0000175833 N0000175835 N0000175980 N0000008556 N0000175089

Packaging Origin

Original Packager
true

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 citrate dextrose a (source: ndc)
Generic Name anhydrous citric acid, dextrose monohydrate, and trisodium citrate dihydrate (source: ndc)
Application Number BN020037 (source: ndc)
Routes
EXTRACORPOREAL
source: ndc

Resolved Composition

Strengths
  • .073 g/10mL
  • .245 g/10mL
  • .22 g/10mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-USE in 1 CASE (23731-6051-1) / 30 mL in 1 VIAL, SINGLE-USE (23731-6051-3)
  • 25 VIAL, SINGLE-USE in 1 CASE (23731-6051-2) / 30 mL in 1 VIAL, SINGLE-USE (23731-6051-3)
  • 30 mL in 1 VIAL, SINGLE-USE (23731-6051-3)
source: ndc

Packages (3)

Ingredients (3)

anhydrous citric acid (.073 g/10mL) dextrose monohydrate (.245 g/10mL) trisodium citrate dihydrate (.22 g/10mL)

Linked Drug Pages (1)

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"}