Anticoagulant Sodium Citrate (trisodium citrate dihydrate) NDC 0338-9669

NDC codes

FDA NDC Directory

Product NDC (as listed)0338-9669Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00338-9669Add 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
0338-9669-01	00338966901	250 mL in 1 BAG (0338-9669-01)Marketed from Apr 2, 2024

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Anticoagulant Sodium Citrate
Generic name (nonproprietary): trisodium citrate dihydrate
Active ingredients: Trisodium citrate dihydrate — 40 mg/mL
Dosage form: Solution
Route: Extracorporeal
Labeler: Baxter Healthcare Corporation
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication BN 980123
Marketing start: Apr 2, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Acidifying Activity (Mechanism)Calcium Chelating Activity (Mechanism)Decreased Coagulation Factor Activity (Physiologic effect)
Identifiers: Product ID 0338-9669_8855e600-2002-4c8b-94dc-d275de33169bSPL ID 8855e600-2002-4c8b-94dc-d275de33169bSPL set ID 7025a0f9-1a56-4416-a3a4-925d755aed90UNII 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

N400338966901 followed by a unit qualifier and the quantity

Package 00338-9669-01. 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 Apr 2, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Anticoagulant Sodium Citrate 4% w/v Solution, USP is intended for use only with automated apheresis devices.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)