FDA.reportPublic FDA data

triCitrasol

Product NDC
23731-6030
11-digit product format
237316030
Labeler code
23731
Product ID
23731-6030_49d76384-a8fa-44ed-99b4-1f75ee4a435d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Trisodium Citrate dihydrate
Dosage form
SOLUTION
Route
EXTRACORPOREAL
Labeler
Citra Labs LLC
Application
BN010409
Marketing category
NDA
Marketing start
2003-07-10
Substance
TRISODIUM CITRATE DIHYDRATE
Active strength
14 g/30mL
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

Additional Listing Data#

Finished product
Yes
Brand name base
triCitrasol
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TRISODIUM CITRATE DIHYDRATE14 g/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
B22547B95KInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
64e7652c-1437-43bd-8ea2-3cafab447b8cAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
23731-6030-12023-02-14triCitrasol ®
23731-6030-22023-02-14triCitrasol ®
23731-6030-12023-01-30triCitrasol ®
23731-6030-22023-01-30triCitrasol ®

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23731-6030-1triCitrasol10 in 1 CASESOLUTION105
23731-6030-2triCitrasol25 in 1 CASESOLUTION255
23731-6030-3triCitrasol30 mL in 1 VIAL, SINGLE-USESOLUTION305

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
23731-6030-3ML - Milliliter23731-60303142e42d-871a-4bc9-931d-90270bc1e87212014-09-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Trisodium Citrate dihydrateACTIVE INGREDIENTB22547B95KTRICITRASOL (TRISODIUM CITRATE DIHYDRATE) SOLUTION [CITRA LABS LLC]2
Anhydrous Citric AcidACTIVE MOIETYXF417D3PSLTRICITRASOL (TRISODIUM CITRATE DIHYDRATE) SOLUTION [CITRA LABS LLC]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
23731-6030TRICITRASOL (TRISODIUM CITRATE DIHYDRATE) SOLUTION [CITRA LABS LLC]5Current NDC, Legacy NDC, 3 package rows20230215_64e7652c-1437-43bd-8ea2-3cafab447b8c.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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
triCitrasolTRISODIUM CITRATE DIHYDRATECitra Labs LLC64e7652c-1437-43bd-8ea2-3cafab447b8c2023-02-14Warnings, Adverse reactionsExact identifier
application number: BN010409
ndc (product): 23731-6030

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
23731-6030-12373160300110 VIAL, SINGLE-USE in 1 CASE (23731-6030-1) / 30 mL in 1 VIAL, SINGLE-USE (23731-6030-3) 2003-07-100000-00-00NoNoCurrent
23731-6030-22373160300225 VIAL, SINGLE-USE in 1 CASE (23731-6030-2) / 30 mL in 1 VIAL, SINGLE-USE (23731-6030-3) 2003-07-100000-00-00NoNoCurrent
23731-6030-32373160300330 mL in 1 VIAL, SINGLE-USE30 mlHistorical