Reliance epoetin
Epoetin alfa and zeta biosimilar developed by Not stated in the CDSCO list. Reference product Eprex (Epogen and Procrit in the United States).
Brands by market: Brand not published by CDSCO (India, import) ยท Commercial partner or holder: Reliance Biopharmaceuticals (import)
FDAnot listed
EMAnot listed
PMDAnot listed
HCnot listed
CDSCOJan 2008permitted
EDEnot listed
Status by market
FDA
United States
Not listed by FDA.
EMA
European Union
Not listed by EMA.
PMDA
Japan
Not listed by PMDA.
HC
Canada
Not listed by HC.
CDSCO
India
Central Drugs Standard Control OrganisationApprovedBrand
Not published by CDSCO (INN only)
Holder or applicant
Reliance Biopharmaceuticals
Pathway
Import and marketing permission
Approved
Jan 2008
Application or permission
Import permission; bulk 31 January 2008
Indications as licensed
Anaemia due to chronic renal failure
Presentations
10,000 IU/mL PFS
Source
S013
EDE
United Arab Emirates
Not listed by EDE.
Chronology
- CDSCOJan 2008CDSCO permission granted
Sources
S013CDSCO, import and market permissions till 2019 (r-DNA) Primary (regulator)
Planning epoetin alfa and zeta biosimilar development?
EvySaif can help assess your regulatory pathway, clinical evidence requirements and market-entry strategy across India, UAE and other target markets.
Talk to a biosimilar regulatory consultantData current to September 2026.