Hetero

Biosimilar developer, India. 5 development products across 5 molecules: adalimumab, bevacizumab, darbepoetin alfa, denosumab, rituximab.

First approval in the Atlas: Jan 2014, Hetero Drugs (INN only), darbepoetin alfa (CDSCO)
FDAproducts approved0
EMAproducts approved0
MHRAproducts approved0
PMDAproducts approved0
HCproducts approved0
CDSCOproducts approved5
EDEproducts registered0

About Hetero

Hetero holds Indian permissions for five biosimilar molecules: darbepoetin, bevacizumab, rituximab, adalimumab and denosumab. Its adalimumab, Mabura, was permitted in 2017 with a full set of uses, and its denosumab is the only Indian product permitted first for the cancer dose. All of its biosimilars are Indian products.

Portfolio by market

MoleculeProductFDAEMAMHRAPMDAHCCDSCOEDEMarkets
AdalimumabMabura·····Jul 2017·1/7
BevacizumabHetero bevacizumab·····May 2016·1/7
Darbepoetin alfaHetero darbepoetin alfa·····Jan 2014·1/7
DenosumabHetero denosumab·····Dec 2024·1/7
RituximabHetero rituximab·····Mar 2015·1/7

Month shown is the first approval or registration of that product in that market.

Companies on the same molecules

Developers whose portfolios overlap most with Hetero, by number of shared molecules. Overlap is the clearest sign of who competes with whom for the same tenders and licensing partners.

Chronology

Compare Hetero with other developers on the comparison page.

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Data current to September 2026.