Sodium Citrate Blood-Pack Units, (PL 146 Plastic) NDC 0942-9505

NDC codes

FDA NDC Directory

Product NDC (as listed)0942-9505Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00942-9505Add 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
0942-9505-10	00942950510	250 mL in 1 BAG (0942-9505-10)Marketed from Mar 1, 2007

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): Sodium Citrate Blood-Pack Units, (PL 146 Plastic)
Generic name (nonproprietary): anticoagulant sodium citrate solution
Active ingredients: Trisodium citrate dihydrate — 4 g/100mL
Dosage form: Solution
Route: Intravenous
Labeler: Fenwal, Inc.
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication BN 770923
Marketing start: Mar 1, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Acidifying Activity (Mechanism)Calcium Chelating Activity (Mechanism)Decreased Coagulation Factor Activity (Physiologic effect)
Identifiers: Product ID 0942-9505_a4ee4dcf-ebb9-4eaa-9630-293e8cd0655eSPL ID a4ee4dcf-ebb9-4eaa-9630-293e8cd0655eSPL set ID a63da38d-1fea-4ee0-a70b-55c891a5ebccUNII 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.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N400942950510 followed by a unit qualifier and the quantity

Package 00942-9505-10. 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 11, 2022.

Full label on DailyMed (opens in a new tab)

Other NDCs under BN 770923

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under BN 770923
Product	Strength	Form · route	Labeler	Product NDC
Sodium Citrate Blood-Pack Units, (PL 146 Plastic)anticoagulant sodium citrate solution	Trisodium citrate dihydrate 4 g/100mL	SolutionIntravenous	Fenwal, Inc.	0942-9504
Sodium Citrate Blood-Pack Units, (PL 146 Plastic)anticoagulant sodium citrate solution	Trisodium citrate dihydrate 4 g/100mL	SolutionIntravenous	Fenwal, Inc.	0942-9506