Medicine
Albuminex 25 g/500 mL injection
Albuminex 25 g/500 mL injection is a prescription medicine containing Albumin human for intravenous use, marketed by Bpl, 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
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
- Albuminex
- Strength
- 25 g/500 mL
- Dosage form
- Injection
- Route
- Intravenous
- Packs
- 1 vial of 500 mL
- Marketing authorisation holder
- Bpl
- Manufacturer
- Bpl
- 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
- 27 May 2020
- Identifiers
- RxCUI 2054221, 2054223, 2054226 +1DailyMed set ID 8428d373-f4b1-4e3b-bb19-ea89048f7c79NDC 64208-2510Application BLA125644
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
| Pack | Code | Labeler | Marketed since |
|---|---|---|---|
| 1 vial, glass in 1 carton / 500 mL in 1 vial, glass | 64208-2510-5 | Bpl | 27 May 2020 |
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.
| Register | Status | Source |
|---|---|---|
| US FDA | Listed, marketed | Source record for this pageChecked 12 November 2026 |
| US FDA | First approved 31 December 1997 | Drugs@FDA |
| EU (EMA) | Not recorded | — |
| India (CDSCO) | Not yet confirmed against CDSCO approval lists | — |
| United States | Registered | US 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/500 mL injection.
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 humanFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- KEDBUMIN prescribing information (Kedrion Sp A) · U.S. National Library of Medicine, DailyMed
Need Albuminex 25 g/500 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.