Procrit (Erythropoietin) NDC 59676-310

Product information

Brand name (proprietary)

Procrit

Generic name (nonproprietary)

erythropoietin

Active ingredients

Epoetin — 10000 [iU]/mL

Dosage form

Injection, Solution

Route

Intravenous, Subcutaneous

Labeler

Janssen Products, LPNDC labeler code 59676

Product type

Prescription drug

Marketing category

BLA — Biologics License ApplicationApplication BLA 103234

Marketing start

Jun 1, 1989

Listing expires

Dec 31, 2026

Other FDA classes

Erythropoietin (Chemical structure)Increased Erythroid Cell Production (Physiologic effect)

Identifiers

Product ID 59676-310_325d5d88-413d-28a2-e063-6394a90a3948SPL ID 325d5d88-413d-28a2-e063-6394a90a3948SPL set ID 0c721ba4-ae19-417f-aae1-221ed1a0866aRxCUI 205913, 205918, 205922, 205924, 212219, 213475, 239998, 239999, 240000, 240377, 241999, 242706, 1721684, 1721690UNII 64FS3BFH5W

Pharmacologic class

Erythropoiesis-stimulating 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

N459676031001 followed by a unit qualifier and the quantity Copy

Package 59676-0310-01. 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

About NDC 59676-310

What is NDC 59676-310?

59676-310 is the product NDC for Procrit (erythropoietin), Epoetin 10000 [iU]/mL injection, solution, listed with the FDA by Janssen Products, LP. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Procrit (Erythropoietin).

What is the active ingredient?

Epoetin.

Who is the labeler?

Janssen Products, LP, NDC labeler code 59676. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Procrit?

6 other product NDCs are listed under this name. See all Procrit NDCs.

Is there a related HCPCS / J-code?

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

Related NDCs: other Procrit products

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

Other NDCs under BLA 103234

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