NDC codes

FDA NDC Directory
Product NDC (as listed)63739-901Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63739-0901Add the package segment from the table below.

Product information

Brand name (proprietary)
Heparin Sodium
Generic name (nonproprietary)
heparin sodium
Active ingredients
Heparin sodium — 5000 [USP'U]/mL
Dosage form
Injection, Solution
Route
Intravenous, Subcutaneous
Labeler
McKesson Corporation dba SKY PackagingNDC labeler code 63739
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202733
Marketing start
Listing expires
Other FDA classes
Heparin (Chemical structure)
Identifiers
Product ID 63739-901_2c31ae6a-f9c6-fb65-e063-6294a90af0e1SPL ID 2c31ae6a-f9c6-fb65-e063-6294a90af0e1SPL set ID 7f05762a-7527-4796-b21e-68277aec379eRxCUI 1361226, 1361574, 1361615, 1362831, 1658647UNII ZZ45AB24CAUPC 0363739986251, 0363739975279, 0363739964259, 0363739942158, 0363739953253, 0363739900264, 0363739920255
Pharmacologic class
Anti-coagulant; Unfractionated Heparin

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

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Heparin sodium injection is indicated for: Prophylaxis and treatment of venous thrombosis and pulmonary embolism; Prevention of postoperative deep venous thrombosis and pulmonary embolism in patients undergoing major abdominothoracic surgery or who, for other reasons, are at risk of developing thromboembolic disease; Atrial fibrillation with embolization; Treatment of acute and chronic consumptive coagulopathies (disseminated intravascular coagulation); Prevention of clotting in arterial and cardiac surgery; Prophylaxis and treatment of peripheral arterial embolism. Anticoagulant use in blood transfusions, extracorporeal circulation, and dialysis procedures. Heparin sodium injection is an an…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63739-901

What is NDC 63739-901?
63739-901 is the product NDC for Heparin Sodium, Heparin sodium 5000 [USP'U]/mL injection, solution, listed with the FDA by McKesson Corporation dba SKY Packaging.
What drug is associated with this NDC?
Heparin Sodium.
What is the active ingredient?
Heparin sodium.
Who is the labeler?
McKesson Corporation dba SKY Packaging, NDC labeler code 63739. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Heparin Sodium?
118 other product NDCs are listed under this name. See all Heparin Sodium NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Heparin Sodium NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Heparin SodiumHeparin sodium 5000 [USP'U]/.5mLInjection, SolutionIntravenous, SubcutaneousCardinal Health 107, LLC55154-958955154-9589-05
Heparin SodiumHeparin sodium 5000 [USP'U]/mLInjectionIntravenous, SubcutaneousREMEDYREPACK INC.70518-454770518-4547-00
Heparin SodiumHeparin sodium 10000 [USP'U]/mLInjectionIntravenous, SubcutaneousMeitheal Pharmaceuticals Inc.71288-45171288-0451-02
Heparin SodiumHeparin sodium 1000 [USP'U]/mLInjectionIntravenous, SubcutaneousMeitheal Pharmaceuticals Inc.71288-44971288-0449-02
Heparin SodiumHeparin sodium 5000 [USP'U]/mLInjectionIntravenous, SubcutaneousMeitheal Pharmaceuticals Inc.71288-45071288-0450-02
Heparin SodiumHeparin sodium 2000 [USP'U]/2mLInjectionIntravenous, SubcutaneousNorthStar RxLLC72603-33672603-0336-25
Heparin SodiumHeparin sodium 5000 [USP'U]/mLInjectionIntravenous, SubcutaneousNorthStar RxLLC72603-41272603-0412-25
Heparin SodiumHeparin sodium 10000 [USP'U]/mLInjectionIntravenous, SubcutaneousNorthStar RxLLC72603-50172603-0501-25
Heparin SodiumHeparin sodium 1000 [USP'U]/mLInjectionIntravenous, SubcutaneousMedical Purchasing Solutions, LLC.71872-735171872-7351-01
Heparin SodiumHeparin sodium 1000 [USP'U]/mLInjectionIntravenous, SubcutaneousMedical Purchasing Solutions, LLC71872-735271872-7352-01

All 119 Heparin Sodium NDCs

Other NDCs under ANDA 202733

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

FDA NDC Directory listings under ANDA 202733
ProductStrengthForm · routeLabelerProduct NDC
Heparin SodiumHeparin sodium 5000 [USP'U]/mLInjection, SolutionIntravenous, SubcutaneousSandoz Inc.0781-3550
Heparin SodiumHeparin sodium 5000 [USP'U]/mLInjection, SolutionIntravenous, SubcutaneousHepalink USA Inc.81952-114

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