Dr. Reddy's Laboratories

Dr. Reddy's Laboratories

RDY
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Private Company

Total funding raised: $100M

Market Cap: $11.1BPipeline: 200 drugs (18 Phase 3)Patents: 20Founded: 1984HQ: Princeton, United States

Overview

Founded in 1984, Dr. Reddy's Laboratories has evolved from an API manufacturer into a global pharmaceutical leader with a mission to accelerate access to affordable and innovative medicines. Its core strategy balances a robust generics and biosimilars business with targeted investments in complex generics, innovative therapies, and strategic partnerships. Key recent achievements include the first-to-market launch of a generic semaglutide injection in India, expansion of its biosimilar portfolio in developed markets, and a stated goal to touch 1.5 billion patient lives by 2030.

OncologyMetabolic Disorders (Diabetes/Obesity)ImmunologyInfectious Diseases (HIV)Central Nervous SystemGastrointestinalPainConsumer Health

Technology Platform

A vertically integrated platform spanning API synthesis, complex generic & biosimilar development (including peptides and monoclonal antibodies), advanced drug delivery, and emerging capabilities in cell & gene therapies.

Pipeline

200
200 drugs in pipeline18 in Phase 3
DrugIndicationStageWatch
Lubiprostone + Lubiprostone + PlaceboChronic Idiopathic ConstipationPhase 3
DRL_RI (Proposed rituximab biosimilar)Follicular LymphomaPhase 3
DFD-03 (0.1% tazarotene) Lotion + DFD-03 (0% tazarotene) Lot...Acne VulgarisPhase 3
AVIGAN + Placebo ComparatorCovid19Phase 3
Abametapir Lotion 0.74% w/w + Vehicle LotionHead Lice InfestationPhase 3

Funding History

2
Total raised:$100M
Debt$100M
IPOUndisclosed

FDA Approved Drugs

44
PREDNISONEANDAOct 1, 2025
ERIBULIN MESYLATEANDAJul 3, 2025
TICAGRELORANDAOct 29, 2024

Company Timeline

1984Founded

Founded in Princeton, United States

2001IPO

Initial Public Offering

2005Debt

Debt: $100.0M

2024FDA Approval

FDA Approval: TICAGRELOR

2025FDA Approval

FDA Approval: PREDNISONE

2025FDA Approval

FDA Approval: ERIBULIN MESYLATE