What is NDC 23731-6030?

23731-6030 is the product NDC for triCitrasol (trisodium citrate dihydrate), Trisodium citrate dihydrate 14 g/30mL solution, listed with the FDA by Citra Labs LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

triCitrasol (Trisodium Citrate dihydrate).

Citra Labs LLC, NDC labeler code 23731. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for triCitrasol?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

triCitrasol NDC 23731-6030 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)23731-6030Labeler and product segments. Claims need a package NDC.

Product NDC at billing width23731-6030Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
23731-6030-1	2373160300123731603001	10 VIAL, SINGLE-USE in 1 CASE (23731-6030-1) / 30 mL in 1 VIAL, SINGLE-USE (23731-6030-3)Marketed from Jul 10, 2003
23731-6030-2	2373160300223731603002	25 VIAL, SINGLE-USE in 1 CASE (23731-6030-2) / 30 mL in 1 VIAL, SINGLE-USE (23731-6030-3)Marketed from Jul 10, 2003

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): triCitrasol
Generic name (nonproprietary): trisodium citrate dihydrate
Active ingredients: Trisodium citrate dihydrate — 14 g/30mL
Dosage form: Solution
Route: Extracorporeal
Labeler: Citra Labs LLCNDC labeler code 23731
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication BN 010409
Marketing start: Jul 10, 2003
Listing expires: Dec 31, 2026
Other FDA classes: Acidifying Activity (Mechanism)Calcium Chelating Activity (Mechanism)Decreased Coagulation Factor Activity (Physiologic effect)
Identifiers: Product ID 23731-6030_49d76384-a8fa-44ed-99b4-1f75ee4a435dSPL ID 49d76384-a8fa-44ed-99b4-1f75ee4a435dSPL set ID 64e7652c-1437-43bd-8ea2-3cafab447b8cUNII B22547B95K
Pharmacologic class: Anti-coagulant; Calculi Dissolution Agent

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N423731603001 followed by a unit qualifier and the quantity

Package 23731-6030-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Feb 14, 2023.

Indications (excerpt from the label)

INDICATIONS AND USAGE triCitrasol ® Anticoagulant Sodium Citrate Concentrate, 46.7% Trisodium Citrate, is an anticoagulant used in granulocytapheresis procedures (granulocyte collection by apheresis). Just prior to performing granulocytapheresis, aseptically add 30 mL of triCitrasol ® to 500 mL of the 6% solution of Hydroxyethyl Starch (HES), e.g. Hespan ® 2-8 . Agitate the resultant solution for 1 minute to assure a uniform concentration of anticoagulant. The resultant solution of triCitrasol ® and 6% solution of HES contains the following concentration depending upon the volume used: Volume of triCitrasol ® Volume of HES Total Volume Final Concentration of triCitrasol ® 30 mL 500 mL (measu…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 23731-6030

What is NDC 23731-6030?: 23731-6030 is the product NDC for triCitrasol (trisodium citrate dihydrate), Trisodium citrate dihydrate 14 g/30mL solution, listed with the FDA by Citra Labs LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: triCitrasol (Trisodium Citrate dihydrate).
What is the active ingredient?: Trisodium citrate dihydrate.
Who is the labeler?: Citra Labs LLC, NDC labeler code 23731. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for triCitrasol?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

triCitrasol (Trisodium citrate dihydrate) NDC 23731-6030