What is NDC 79403-791?

79403-791 is the product NDC for Pall Sterile Cord Blood Collection Unit, Sodium citrate .921 g/35mL + 3 more ingredients solution, listed with the FDA by Global Life Sciences Solutions USA LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Pall Sterile Cord Blood Collection Unit (Sterile Cord Blood Collection Unit).

What is the active ingredient?

Sodium citrate, Citric acid monohydrate, Sodium phosphate, Monobasic, Monohydrate, Dextrose monohydrate.

Global Life Sciences Solutions USA LLC, NDC labeler code 79403. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Pall Sterile Cord Blood Collection Unit?

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.

Pall Sterile Cord Blood Collection Unit NDC 79403-791

NDC codes

FDA NDC Directory

Product NDC (as listed)79403-791Labeler and product segments. Claims need a package NDC.

Product NDC at billing width79403-0791Add 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
79403-791-08	79403079108	35 mL in 1 BAG (79403-791-08)Marketed from Dec 18, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Pall Sterile Cord Blood Collection Unit
Generic name (nonproprietary): sterile cord blood collection unit
Active ingredients: Sodium citrate — .921 g/35mLCitric acid monohydrate — .114 g/35mLSodium phosphate, Monobasic, Monohydrate — .0078 g/35mLDextrose monohydrate — .893 g/35mL
Dosage form: Solution
Route: Intravenous
Labeler: Global Life Sciences Solutions USA LLCNDC labeler code 79403
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication BN 800222
Marketing start: Dec 18, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Acidifying Activity (Mechanism)Acidifying Activity (Mechanism)Calcium Chelating Activity (Mechanism)Calcium Chelating Activity (Mechanism)Decreased Coagulation Factor Activity (Physiologic effect)Decreased Coagulation Factor Activity (Physiologic effect)
Identifiers: Product ID 79403-791_46366161-f003-2826-e063-6394a90a91a5SPL ID 46366161-f003-2826-e063-6394a90a91a5SPL set ID aa9340b7-cc63-e17d-e053-2a95a90ad4d9UNII 1Q73Q2JULR, 2968PHW8QP, 593YOG76RN, LX22YL083G
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

N479403079108 followed by a unit qualifier and the quantity

Package 79403-0791-08. 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 Dec 18, 2025.

Indications (excerpt from the label)

Indications and Usage Section For collection of up to 210 ml of umbilical cord blood. Use aseptic technique. Contents inside overwrap pouch, within the foil envelope, are sterile and acceptable for use in a sterile field if pouch is unopened and undamaged; visual inspection to confirm the integrity of overwrap pouch should be performed.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 79403-791

What is NDC 79403-791?: 79403-791 is the product NDC for Pall Sterile Cord Blood Collection Unit, Sodium citrate .921 g/35mL + 3 more ingredients solution, listed with the FDA by Global Life Sciences Solutions USA LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pall Sterile Cord Blood Collection Unit (Sterile Cord Blood Collection Unit).
What is the active ingredient?: Sodium citrate, Citric acid monohydrate, Sodium phosphate, Monobasic, Monohydrate, Dextrose monohydrate.
Who is the labeler?: Global Life Sciences Solutions USA LLC, NDC labeler code 79403. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pall Sterile Cord Blood Collection Unit?: 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.

Pall Sterile Cord Blood Collection Unit (Sterile cord blood collection unit) NDC 79403-791