Ranopto

Ranibizumab biosimilar developed by Teva Canada. Reference product Lucentis.

Brands by market: Ranopto (Canada) · Commercial partner or holder: Teva Canada · Company profile
FDANot listed
EMANot listed
MHRANot listed
PMDANot listed
HCOct 2023approved
CDSCONot listed
EDENot listed
Approved or registered in 1 of 7 markets

About Ranopto

Ranopto is Teva's ranibizumab for Canada, approved in October 2023. Teva has not named the developer of the product, and it has no counterpart in the United States or Europe.

Status by market

FDA

United States

Not listed by FDA.

EMA

European Union

Not listed by EMA.

MHRA

United Kingdom

Not listed by MHRA.

PMDA

Japan

Not listed by PMDA.

HC

Canada · Ranopto

Health CanadaApproved
Brand
Ranopto
Holder or applicant
Teva Canada Limited
Pathway
Biosimilar biologic drug (Notice of Compliance)
Approved
Oct 2023
Application or permission
DIN 02542250
Presentations
10 mg
Source
S022 (Health Canada) · checked Sep 2026
CDSCO

India

Not listed by CDSCO.

EDE

United Arab Emirates

Not listed by EDE.

Other developers in the same markets

Where Ranopto holds an approval, these are the other ranibizumab biosimilars approved in that market.

MarketRivalsDevelopers (product)
HC1Samsung Bioepis (Byooviz)

Same developer, other molecules

Other biosimilars in the Atlas developed by Teva: Ovaleap, Ponlimsi / Degevma, Teriparatide Teva, Tevagrastim / Ratiograstim.

Chronology

Sources

All ranibizumab biosimilars

Planning ranibizumab 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 consultant
Data current to September 2026.