Search for high-quality Active Pharmaceutical Ingredients through our extensive portfolio
Why Choose Us
API Solutions
The Dr. Reddy’s API business is a leading manufacturer and supplier of high quality affordable Active Pharmaceutical Ingredients (API) to leading generic formulations manufacturers across the world, enabling them to accelerate access to affordable medicines for patients worldwide. We offer 250+ affordable, high-quality APIs in over 80+ countries. Backed by decades of R&D strength, the focus is on first-to-market, hard-to-make products, driven by sustainability and high standards in quality, safety, supply and productivity.
Your Trusted Partner for High-Quality, Affordable APIs
Dr. Reddy’s API business is a leading manufacturer and supplier of high-quality quality affordable Active Pharmaceutical Ingredients (APIs) to leading generic formulations manufacturers across the world, enabling them to accelerate access to affordable medicines for patients worldwide. As a preferred partner across major markets, we lead with sustainability, first-to-market products, and an unwavering commitment to quality.
Why work with us
Years of serving patients
Active pharmaceutical Ingredients
DMFs filed globally
Billion USD Revenue
Countries presence
API manufacturing sites
As nossas capacidades
Advanced Research Capabilities
Reddy's compreende fortes equipes técnicas e multifuncionais, incluindo departamentos de P&D, Qualidade, Engenharia e Análise. Nossas equipes dedicadas de P&D estão comprometidas em desenvolver produtos complexos para atender às crescentes necessidades de API no ambiente GMP.
Regulatory Compliance
O Dr. Reddy tem uma experiência regulatória global incomparável focada em mercados internacionais. Nossa qualidade de primeira classe e conformidade líder do setor são projetadas para garantir que nossos produtos atendam aos rigorosos requisitos regulatórios em todo o mundo. Nossas APIs possuem registros regulatórios disponíveis nos principais mercados do mundo.
Manufacturing Excellence
Our API manufacturing facilities are operated following cGMP (ICH Q7) and regularly inspected by international regulatory authorities. We have eight commercial USFDA inspected production units, six in India, one in Mexico and one in the UK.
Our Journey in Motion
Eventos e Prémios
A Bold Leap for Global HIV Prevention: Lenacapavir Agreement SignedTentative Approval for Generic Lumateperone capsules
Thrilled to announce that we’ve officially signed the agreement for Lenacapavir with UNITAID, CHAI, and Wits RHI. Together, we are making Lenacapavir, a twice-yearly HIV prevention injection available...
Tentative Approval for Generic Lumateperone capsules
CDP Recognition
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