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Medicine

Kedbumin 25 g/100 mL injection

Albumin human · Intravenous · Kedrion Sp A
Available on requestPrescription onlyUS FDA

Kedbumin 25 g/100 mL injection is a prescription medicine containing Albumin human for intravenous use, marketed by Kedrion Sp A, 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.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Ambient

Do not freeze. Do not store above 30°C (86° F). Keep the vial stored in the…

Key facts

Active ingredient (INN)
Albumin human
Brand
Kedbumin
Strength
25 g/100 mL
Dosage form
Injection
Route
Intravenous
Packs
1 vial of 100 mL
Marketing authorisation holder
Kedrion Sp A
Manufacturer
Kedrion Sp A
Origin register
US FDA, United States
Storage
Do not freeze. Do not store above 30°C (86° F). Keep the vial stored in the outer carton in order to protect from light.
Cold chain
Not required on record
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
15 September 2011
Identifiers
RxCUI 1741375, 1741380, 1742222 +1DailyMed set ID 57bd6811-8619-11e0-9d78-0800200c9a66NDC 76179-025Application BLA125384

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 vial in 1 carton / 100 mL in 1 vial76179-025-04Kedrion Sp A15 September 2011

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
US FDAFirst approved 31 December 1997Drugs@FDA
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

Alternatives

Other makers and brands of Albumin human 25 g/100 mL injection.

Compare all 7

Other strengths and forms of Albumin human

Clinical summary

Albumin human is a human serum albumin indicated for hypovolemia and Hypoalbuminemia, among other approved uses. It is available as injection for intravenous use. MedsAcross supplies Albumin human 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 Albumin human

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

Data sources

Need Kedbumin 25 g/100 mL injection 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.