Home NDC 23731-6051 Anticoagulant Citrate Dextrose A
Product NDC 23731-6051
11-digit product format 237316051
Labeler code 23731
Product ID 23731-6051_9a133b17-0377-431f-b839-3e090fdabd78
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Anhydrous Citric Acid, Dextrose Monohydrate, and Trisodium Citrate Dihydrate
Dosage form SOLUTION
Route EXTRACORPOREAL
Labeler Citra Labs LLC
Application BN020037
Marketing category NDA
Marketing start 2003-08-26
Substance ANHYDROUS CITRIC ACID; DEXTROSE MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE
Active strength .073; .245; .22 g/10mL; g/10mL; g/10mL
Pharmacologic classes 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]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Anticoagulant Citrate Dextrose A
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DEXTROSE MONOHYDRATE .073 g/10mL ANHYDROUS CITRIC ACID .245 g/10mL TRISODIUM CITRATE DIHYDRATE .22 g/10mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination LX22YL083G Internal UNII lookup XF417D3PSL Internal UNII lookup B22547B95K Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# NDC, Effective, Related label table NDC Effective Related label 23731-6051-1 2023-02-14 ACD-A Anticoagulant Citrate Dextrose Solution, Solution A, U.S.P., PN 9350, 30 mL NDC 23731-6051-3 23731-6051-2 2023-02-14 ACD-A Anticoagulant Citrate Dextrose Solution, Solution A, U.S.P., PN 9350, 30 mL NDC 23731-6051-3 23731-6051-3 2023-02-14 ACD-A Anticoagulant Citrate Dextrose Solution, Solution A, U.S.P., PN 9350, 30 mL NDC 23731-6051-3 23731-6051-1 2023-01-30 ACD-A Anticoagulant Citrate Dextrose Solution, Solution A, U.S.P., PN 9350, 30 mL NDC 23731-6051-3 23731-6051-2 2023-01-30 ACD-A Anticoagulant Citrate Dextrose Solution, Solution A, U.S.P., PN 9350, 30 mL NDC 23731-6051-3 23731-6051-3 2023-01-30 ACD-A Anticoagulant Citrate Dextrose Solution, Solution A, U.S.P., PN 9350, 30 mL NDC 23731-6051-3
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 23731-6051-1 Anticoagulant Citrate Dextrose A 10 in 1 CASE SOLUTION 10 5 23731-6051-2 Anticoagulant Citrate Dextrose A 25 in 1 CASE SOLUTION 25 5 23731-6051-3 Anticoagulant Citrate Dextrose A 30 mL in 1 VIAL, SINGLE-USE SOLUTION 30 5
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Anhydrous Citric Acid ACTIVE INGREDIENT XF417D3PSL ANTICOAGULANT CITRATE DEXTROSE A (ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATE) SOLUTION [CITRA LABS] 2 Dextrose Monohydrate ACTIVE INGREDIENT LX22YL083G ANTICOAGULANT CITRATE DEXTROSE A (ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATE) SOLUTION [CITRA LABS] 2 Trisodium Citrate Dihydrate ACTIVE INGREDIENT B22547B95K ANTICOAGULANT CITRATE DEXTROSE A (ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATE) SOLUTION [CITRA LABS] 2 Anhydrous Citric Acid ACTIVE MOIETY XF417D3PSL ANTICOAGULANT CITRATE DEXTROSE A (ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATE) SOLUTION [CITRA LABS] 2 Anhydrous Dextrose ACTIVE MOIETY 5SL0G7R0OK ANTICOAGULANT CITRATE DEXTROSE A (ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATE) SOLUTION [CITRA LABS] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 23731-6051 ANTICOAGULANT CITRATE DEXTROSE A (ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATE) SOLUTION [CITRA LABS LLC] 5 Current NDC, Legacy NDC, 3 package rows 20230215_5bcd261e-ebba-4ecb-af22-e5aaeb04499b.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 23731-6051-1 23731605101 10 VIAL, SINGLE-USE in 1 CASE (23731-6051-1) / 30 mL in 1 VIAL, SINGLE-USE (23731-6051-3) 2003-08-26 0000-00-00 No No Current 23731-6051-2 23731605102 25 VIAL, SINGLE-USE in 1 CASE (23731-6051-2) / 30 mL in 1 VIAL, SINGLE-USE (23731-6051-3) 2003-08-26 0000-00-00 No No Current 23731-6051-3 23731605103 30 mL in 1 VIAL, SINGLE-USE (23731-6051-3) 30 ml 2003-08-26 0000-00-00 No No Current