Dr. Reddy's: Leading the Way

Published Online: Thursday, August 30, 2012
Follow Pharmacy_Times:


Dr. Reddy’s is a vertically integrated global pharmaceutical company and is among the leaders in the supply of generic active pharmaceutical ingredients (APIs) worldwide. It is the first non-Japanese Asian company listed on the NYSE (RDY). It currently has sales revenues of $2 billion. There are 8 API facilities globally, which are FDA-inspected, and 4 FDA-approved finished dosage facilities servicing the United States.

Through its 3 businesses—Pharmaceutical Services and Active Ingredients, Global Generics, and Proprietary Products—it offers a portfolio of products and services, including APIs, Custom Pharmaceutical Services (CPS), generics, differentiated formulations, and New Chemical Entities (NCEs). Dr. Reddy’s has 13 facilities, including API and finished dosage manufacturing.

At a glance:
  • 50 prescription products are marketed under the Dr. Reddy’s label in 250+ dosing presentations
  • 10 OTC products are marketed in 200+ store-brand packaging presentations (private label)
  • Robust pipeline: 76 ANDAs are pending, of which 40 are Para IV certifications, with 15 tentative approvals and 10 FTFs
  • 26 Rx products are ranked top 3 in market sharea
  • Dr. Reddy’s ranks #10 in total generic prescription volume over the last yearb
  • 14,500+ associates worldwide
With our continuing investments in product development, aggressive acquisitions, and advances in research, processes, and technologies, we’re meeting the demands of a changing market. We have the capabilities to help overcome market entry barriers, such as formulation, manufacturing, API, delivery method, and intellectual property. We are also uniquely positioned to support Rx-to-OTC switches.

Discover for yourself how our diverse line of generics, OTCs, and other affordable medicines can make the difference. Make Dr. Reddy’s your low-cost provider of quality pharmaceutical products.

aIMS Volumes, February 2012
bIMS data dispensed generic TRx MAT, March 2012


For more information, visit www.drreddys.com.

Related Articles
A California drug manufacturer must recall and destroy all of its dietary supplements after a federal court determined that it failed to follow FDA manufacturing practice regulations.
Cardinal Health plans to release second-quarter financial results for its fiscal year 2015 on Jan. 29, prior to the opening of trading on the New York Stock Exchange.
A supplemental new drug application for the use of Vertex Pharmaceuticals’ ivacaftor in cystic fibrosis patients aged 6 years and older who have the R117H mutation in the cystic fibrosis transmembrane conductance regulator gene has been approved by the FDA.
Teva Pharmaceutical Industries Ltd. announces the launch of the first FDA-approved generic equivalent to Celebrex Capsules in the United States.
Latest Issues
  • photo
    Pharmacy Times
    photo
    Health-System Edition
    photo
    Directions in Pharmacy
    photo
    OTC Guide
    photo
    Generic Supplements
  • photo
    Pharmacy Careers
    photo
    Specialty Pharmacy Times
    photo
    Generic
$auto_registration$