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Reliance Life Sciences

Biosimilar developer, India. 14 development products across 14 molecules: adalimumab, bevacizumab, darbepoetin alfa, denosumab, etanercept, follitropin alfa, golimumab, infliximab, omalizumab, ranibizumab, rituximab, somatropin, trastuzumab, ustekinumab.

First approval in the Atlas: Apr 2010, Reliance Life Sciences (INN only), follitropin alfa (CDSCO)
FDAproducts approved0
EMAproducts approved0
MHRAproducts approved0
PMDAproducts approved0
HCproducts approved0
CDSCOproducts approved14
EDEproducts registered0

About Reliance Life Sciences

Reliance Life Sciences holds more Indian biosimilar permissions than any other company: fourteen molecules, from follitropin in 2010 to golimumab and ustekinumab in 2023. It was the first company in the world to receive permissions for bevacizumab, golimumab and omalizumab, and the first domestic Indian maker of infliximab. All of its products are sold in India, and none has yet been filed with the regulators in the United States, Europe, Japan, Canada or the Gulf. Its ustekinumab, UstekiRel, is one of the few Indian permissions where the published record names the brand.

Portfolio by market

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

Also holds or markets

Products developed by another company for which Reliance Life Sciences is the licence holder or applicant in one or more markets.

MoleculeBrandMarketHolder or applicantApprovedDeveloper
Epoetin alfa and zetaReliance Biopharmaceuticals (INN only)CDSCOReliance BiopharmaceuticalsJan 2008Not stated in the CDSCO list

Companies on the same molecules

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

Chronology

Compare Reliance Life Sciences with other developers on the comparison page.

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Data current to September 2026.