Teriparatide Dr. Reddy's
Teriparatide biosimilar developed by Dr. Reddy's Laboratories. Reference product Forsteo (Forteo in the United States).
Brands by market: Teriparatide Dr. Reddy's (UK) · Commercial partner or holder: Dr. Reddy's Laboratories · Company profile
FDANot listed
EMANot listed
MHRALicenseddate not shown
PMDANot listed
HCNot listed
CDSCONot listed
EDENot listed
Approved or registered in 1 of 7 markets
About Teriparatide Dr. Reddy's
Teriparatide Dr. Reddy's is Dr. Reddy's teriparatide for the United Kingdom, licensed as a pre-filled pen under the company's name rather than a brand. It adds to the company's rituximab, approved in Europe and the United States.
Status by market
FDA
United States
Not listed by FDA.
EMA
European Union
Not listed by EMA.
MHRA
United Kingdom · Teriparatide Dr. Reddy's
Medicines and Healthcare products Regulatory AgencyApprovedBrand
Teriparatide Dr. Reddy's
Holder or applicant
Not shown in the MHRA substance list
Pathway
UK marketing authorisation (Great Britain and, for EU-converted licences, Northern Ireland)
Approved
not published
Presentations
20 micrograms/80 microlitres pen
Source
S023 (MHRA Products) · checked Sep 2026
PMDA
Japan
Not listed by PMDA.
HC
Canada
Not listed by HC.
CDSCO
India
Not listed by CDSCO.
EDE
United Arab Emirates
Not listed by EDE.
Chronology
Sources
S023MHRA Products, substance lists of licensed medicines (products.mhra.gov.uk) Primary (regulator)
Planning teriparatide 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.