Home NDC 0942-9201 Anticoagulant Citrate Phosphate Dextrose (CPD) Blood-Pack Units in PL 146 Plastic
Product NDC 0942-9201
11-digit product format 009429201
Labeler code 0942
Product ID 0942-9201_1ee1e424-2028-4b58-b554-883d2e359c28
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Anticoagulant Citrate Phosphate Dextrose (CPD) Solution
Dosage form SOLUTION
Route INTRAVENOUS
Labeler Fenwal, Inc.
Application BN170401
Marketing category NDA
Marketing start 2007-03-01
Substance ANHYDROUS CITRIC ACID; DEXTROSE MONOHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE
Active strength 105; 893; 78; 921 mg/35mL; mg/35mL; mg/35mL; mg/35mL
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 Phosphate Dextrose (CPD) Blood-Pack Units in PL 146 Plastic
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TRISODIUM CITRATE DIHYDRATE 105 mg/35mL DEXTROSE MONOHYDRATE 893 mg/35mL ANHYDROUS CITRIC ACID 78 mg/35mL SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE 921 mg/35mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 0942-9201-01 Anticoagulant Citrate Phosphate Dextrose (CPD) Blood-Pack Units in PL 146 Plastic 35 mL in 1 BAG SOLUTION 35 8
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ANHYDROUS CITRIC ACID ACTIVE INGREDIENT XF417D3PSL ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) BLOOD-PACK UNITS IN PL 146 PLASTIC (ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) SOLUTION) SOLUTION [FENWAL, INC.] 6 DEXTROSE MONOHYDRATE ACTIVE INGREDIENT LX22YL083G ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) BLOOD-PACK UNITS IN PL 146 PLASTIC (ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) SOLUTION) SOLUTION [FENWAL, INC.] 6 SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE ACTIVE INGREDIENT 593YOG76RN ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) BLOOD-PACK UNITS IN PL 146 PLASTIC (ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) SOLUTION) SOLUTION [FENWAL, INC.] 6 TRISODIUM CITRATE DIHYDRATE ACTIVE INGREDIENT B22547B95K ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) BLOOD-PACK UNITS IN PL 146 PLASTIC (ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) SOLUTION) SOLUTION [FENWAL, INC.] 6 Anhydrous Citric Acid ACTIVE MOIETY XF417D3PSL ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) BLOOD-PACK UNITS IN PL 146 PLASTIC (ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) SOLUTION) SOLUTION [FENWAL, INC.] 6 ANHYDROUS DEXTROSE ACTIVE MOIETY 5SL0G7R0OK ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) BLOOD-PACK UNITS IN PL 146 PLASTIC (ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) SOLUTION) SOLUTION [FENWAL, INC.] 6 PHOSPHATE ION ACTIVE MOIETY NK08V8K8HR ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) BLOOD-PACK UNITS IN PL 146 PLASTIC (ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) SOLUTION) SOLUTION [FENWAL, INC.] 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0942-9201 ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) BLOOD-PACK UNITS IN PL 146 PLASTIC (ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) SOLUTION) SOLUTION [FENWAL, INC.] 8 Current NDC, Legacy NDC, 1 package rows 20221102_d55cb701-9664-4931-8754-1a8cae68da06.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 0942-9201-01 00942920101 35 mL in 1 BAG (0942-9201-01) 35 ml 2007-03-01 0000-00-00 No No Current