Home NDC 14537-883 Sodium Citrate w/v Anticoagulant
Product NDC 14537-883
11-digit product format 145370883
Labeler code 14537
Product ID 14537-883_4e4eaf1d-b071-4ee8-83ea-739e6388b3b4
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name TRISODIUM CITRATE DIHYDRATE
Dosage form INJECTION, SOLUTION
Route INTRAVENOUS
Labeler Terumo BCT, Ltd
Application BA125608
Marketing category ANDA
Marketing start 2018-06-26
Substance TRISODIUM CITRATE DIHYDRATE
Active strength 4 g/100mL
Pharmacologic classes Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE]
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 14537-883-03 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 14537-883-03 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base Sodium Citrate w/v Anticoagulant
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TRISODIUM CITRATE DIHYDRATE 4 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination B22547B95K Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 14537-883-00 Sodium Citrate w/v Anticoagulant 250 mL in 1 BAG INJECTION, SOLUTION 250 2 14537-883-03 Sodium Citrate w/v Anticoagulant 30 in 1 CARTON INJECTION, SOLUTION 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 14537-883 SODIUM CITRATE W/V ANTICOAGULANT (TRISODIUM CITRATE DIHYDRATE) INJECTION, SOLUTION [TERUMO BCT, LTD] 2 Current NDC, Legacy NDC, 2 package rows 20250129_c9d0e9c8-379f-4895-b272-329efab575c4.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 14537-883-00 14537088300 250 mL in 1 BAG 250 ml Historical 14537-883-03 14537088303 30 BAG in 1 CARTON (14537-883-03) / 250 mL in 1 BAG (14537-883-00) 30 bag 2018-06-26 0000-00-00 No No Current