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MedsAcross

Medicine

Rebinyn kit

Available on requestPrescription onlyUS FDA Cold chain

Rebinyn kit is a prescription medicine containing Coagulation factor ix recombinant, marketed by Novo Nordisk, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians. It ships in a temperature-controlled cold chain.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Cold chain

Store REBINYN in the original package in order to protect from light. • Store…

Key facts

Active ingredient (INN)
Coagulation factor ix recombinant
Brand
Rebinyn
Dosage form
Kit
Packs
1 kit and 1 more
Marketing authorisation holder
Novo Nordisk
Manufacturer
Novo Nordisk
Origin register
US FDA, United States
Storage
Store REBINYN in the original package in order to protect from light. • Store REBINYN under refrigeration at a temperature of 36°F-46°F (2°C – 8°C) for up to 24 months from the date of manufacture until the expiration date stated on the label. • REBINYN may be stored at room temperature not to exceed 86°F (30°C) for up to 6 months within the 24-month time period.
Cold chain
Yes, shipped temperature controlled
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
HS code (indicative)
3002.12Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
1 December 2017
Identifiers
RxCUI 1990857, 1990862DailyMed set ID 0ea37235-35fd-410d-b8c4-40ba15fe1294NDC 0169-7905, 0169-7902, 0169-7901 +1Application BLA125611

Record updated 12 November 2026

Documents available

Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.

No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.

Packs

PackCodeLabelerMarketed since
1 kit in 1 kit * 4 mL in 1 vial, glass * 4 mL in 1 syringe, glass * 4 mL in 1 vial, glass0169-7901-01Novo Nordisk1 December 2017
1 kit in 1 kit * 4 mL in 1 vial, glass * 4 mL in 1 syringe, glass * 4 mL in 1 vial, glass0169-7902-01Novo Nordisk1 December 2017
1 kit in 1 kit * 4 mL in 1 vial, glass * 4 mL in 1 syringe, glass0169-7903-01Novo Nordisk11 August 2022
1 kit in 1 kit * 4 mL in 1 vial, glass * 4 mL in 1 syringe, glass * 4 mL in 1 vial, glass0169-7905-01Novo Nordisk1 December 2017

Status by register

Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.

RegisterStatusSource
US FDAListed, marketedSource record for this pageChecked 12 November 2026
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Import route

Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.

Import guides are available for 25 countries. Pick one to see its route summary.

BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides

Clinical summary

Coagulation factor ix recombinant is a prescription medicine indicated in adults and children with hemophilia B (congenital Factor IX deficiency) for on-demand treatment and control of bleeding episodes, among other approved uses. MedsAcross supplies Coagulation factor ix recombinant for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Read about Coagulation factor ix recombinant

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

Data sources

Need Rebinyn kit for your hospital or patient?

Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.