Home NDC 43203-852 Anticoagulant Citrate Dextrose A ACD-A
Product NDC 43203-852
11-digit product format 432030852
Labeler code 43203
Product ID 43203-852_49c60185-a86d-44a7-a10e-d0ec57df1fbe
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Anticoagulant Citrate Dextrose A ACD-A
Dosage form INJECTION, SOLUTION
Route EXTRACORPOREAL
Labeler Arteriocyte Medical Systems, Inc.
Application BA110057
Marketing category ANDA
Marketing start 2011-05-11
Substance CITRIC ACID MONOHYDRATE; DEXTROSE MONOHYDRATE; SODIUM CITRATE, UNSPECIFIED FORM
Active strength .08; .245; .22 g/10mL; g/10mL; g/10mL
Pharmacologic classes Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 43203-852-47 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 43203-852-47 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Anticoagulant Citrate Dextrose A ACD-A
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CITRIC ACID MONOHYDRATE .08 g/10mL SODIUM CITRATE, UNSPECIFIED FORM .22 g/10mL DEXTROSE MONOHYDRATE .245 g/10mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2968PHW8QP Internal UNII lookup 1Q73Q2JULR Internal UNII lookup LX22YL083G Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43203-852-47 Anticoagulant Citrate Dextrose A ACD-A 1 in 1 POUCH INJECTION, SOLUTION 1 4 43203-852-47 Anticoagulant Citrate Dextrose A ACD-A 50 in 1 CASE INJECTION, SOLUTION 50 4
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CITRIC ACID MONOHYDRATE ACTIVE INGREDIENT 2968PHW8QP ANTICOAGULANT CITRATE DEXTROSE A ACD-A INJECTION, SOLUTION [ARTERIOCYTE MEDICAL SYSTEMS, INC.] 2 DEXTROSE MONOHYDRATE ACTIVE INGREDIENT LX22YL083G ANTICOAGULANT CITRATE DEXTROSE A ACD-A INJECTION, SOLUTION [ARTERIOCYTE MEDICAL SYSTEMS, INC.] 2 SODIUM CITRATE ACTIVE INGREDIENT 1Q73Q2JULR ANTICOAGULANT CITRATE DEXTROSE A ACD-A INJECTION, SOLUTION [ARTERIOCYTE MEDICAL SYSTEMS, INC.] 2 ANHYDROUS CITRIC ACID ACTIVE MOIETY XF417D3PSL ANTICOAGULANT CITRATE DEXTROSE A ACD-A INJECTION, SOLUTION [ARTERIOCYTE MEDICAL SYSTEMS, INC.] 2 ANHYDROUS DEXTROSE ACTIVE MOIETY 5SL0G7R0OK ANTICOAGULANT CITRATE DEXTROSE A ACD-A INJECTION, SOLUTION [ARTERIOCYTE MEDICAL SYSTEMS, INC.] 2 SODIUM CATION ACTIVE MOIETY LYR4M0NH37 ANTICOAGULANT CITRATE DEXTROSE A ACD-A INJECTION, SOLUTION [ARTERIOCYTE MEDICAL SYSTEMS, INC.] 2 Water INACTIVE INGREDIENT 059QF0KO0R ANTICOAGULANT CITRATE DEXTROSE A ACD-A INJECTION, SOLUTION [ARTERIOCYTE MEDICAL SYSTEMS, INC.] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43203-852 ANTICOAGULANT CITRATE DEXTROSE A ACD-A INJECTION, SOLUTION [ARTERIOCYTE MEDICAL SYSTEMS, INC.] 4 Current NDC, Legacy NDC, 2 package rows 20250125_b850deac-161f-4bb0-ac7f-bceac2a230c0.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 · 2 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 43203-852-47 43203085247 50 POUCH in 1 CASE (43203-852-47) / 1 BAG in 1 POUCH / 50 mL in 1 BAG 50 pouch 2011-05-11 0000-00-00 No No Current