Eloctate NDC 71104-805

Product information

Brand name (proprietary)

Eloctate

Generic name (nonproprietary)

antihemophilic factor (recombinant), fc fusion protein

Dosage form

Kit

Route

Intravenous

Labeler

Bioverativ Therapeutics Inc.NDC labeler code 71104

Product type

Plasma derivative

Marketing category

BLA — Biologics License ApplicationApplication BLA 125487

Marketing start

Sep 6, 2017

Listing expires

Dec 31, 2026

Identifiers

Product ID 71104-805_e600c559-32d8-4818-b600-141cc0d74ceaSPL ID e600c559-32d8-4818-b600-141cc0d74cea

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

N471104080501 followed by a unit qualifier and the quantity Copy

Package 71104-0805-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 71104-805

What is NDC 71104-805?

71104-805 is the product NDC for Eloctate kit, listed with the FDA by Bioverativ Therapeutics Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Eloctate (Antihemophilic Factor (Recombinant), Fc Fusion Protein).

Who is the labeler?

Bioverativ Therapeutics Inc., NDC labeler code 71104. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Eloctate?

9 other product NDCs are listed under this name. See all Eloctate NDCs.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory. See Billing references above.

Related NDCs: other Eloctate products

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

Other NDCs under BLA 125487

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