MedPath

DR. REDDY'S LABORATORIES, INC.

DR. REDDY'S LABORATORIES, INC. logo
🇺🇸United States
Ownership
Subsidiary
Employees
-
Market Cap
-
Website
http://www.drreddys.com

Clinical Trials

2

Active:0
Completed:1

Trial Phases

1 Phases

Not Applicable:2

Drug Approvals

156

FDA:126
CANADA:15

Drug Approvals

Lamotrigine

Approval Date
Aug 1, 2025
FDA

Fexofenadine Hydrochloride

Approval Date
May 2, 2025
FDA

varenicline tartrate

Approval Date
Mar 31, 2025
FDA

Ticagrelor

Approval Date
Nov 13, 2024
FDA

Atorvastatin Calcium

Approval Date
Mar 22, 2024
FDA

Liothyronine Sodium

Approval Date
Mar 15, 2024
FDA

DISOPYRAMIDE PHOSPHATE

Approval Date
Mar 1, 2024
FDA

Amiodarone Hydrochloride

Approval Date
Mar 1, 2024
FDA

ERRIN

Approval Date
Mar 1, 2024
FDA

Famotidine

Approval Date
Feb 22, 2024
FDA
  • Prev
  • 1
  • 2
  • 3
  • 4
  • 5
  • 13
  • Next

Clinical Trials

Distribution across different clinical trial phases (2 trials with phase data)• Click on a phase to view related trials

Not Applicable
2 (100.0%)
No trials found

News

Dr. Reddy's Launches Next-Generation Acid Blocker Tegoprazan in India Following Phase III Success

Dr. Reddy's Laboratories has launched tegoprazan, a next-generation potassium-competitive acid blocker (PCAB), in India for treating acid peptic diseases including GERD and gastric ulcers.

Dr. Reddy's Laboratories Acquires Johnson & Johnson's STUGERON Brand for $50.5 Million to Expand CNS Portfolio

Dr. Reddy's Laboratories has acquired the STUGERON brand from Johnson & Johnson for $50.5 million, expanding its central nervous system therapeutic portfolio across 18 markets in Asia-Pacific and EMEA regions.

Alvotech Reports Record First Half 2025 Results with Over 200% Product Revenue Growth

Alvotech achieved over 200% year-on-year growth in product revenues for the first six months of 2025, reaching $204.7 million compared to $65.9 million in the same period of 2024.

Granules India CEO Dr. K V Sitaram Rao Announces Resignation Effective July 2025

Dr. Kandiraju Venkata Sitaram Rao has resigned from his position as Joint Managing Director and CEO of Granules India Limited, effective July 31, 2025.

Dr. Reddy's and Alvotech Partner to Develop Keytruda Biosimilar in $29.5 Billion Market

Dr. Reddy's Laboratories and Alvotech have entered a collaboration and license agreement to co-develop, manufacture, and commercialize a biosimilar version of Keytruda (pembrolizumab) for global markets.

Eisai and Merck Secure Patent Victory, Blocking Lenvima Generic Until 2036

Eisai and Merck successfully defended a key patent for cancer drug Lenvima against Shilpa Medicare's challenge, with a federal judge ruling the patent describes the invention clearly and in sufficient detail.

USFDA Issues Form 483 with Two Observations for Dr. Reddy's New York API Facility

The U.S. Food and Drug Administration completed a Good Manufacturing Practice inspection at Dr. Reddy's Middleburgh API facility in New York, resulting in two observations via Form 483.

Esperion Secures Patent Protection for NEXLETOL Until 2040 Through Settlement with Micro Labs

Esperion Therapeutics has reached a settlement agreement with Micro Labs that prevents the generic manufacturer from marketing a version of NEXLETOL (bempedoic acid) before April 19, 2040.

Ingenus Pharmaceuticals Advances Cancer Drug Patent Suit Against Nexus, Court Dismisses Co-Plaintiff

A federal judge in Illinois ruled that Ingenus Pharmaceuticals can proceed with its patent infringement lawsuit against Nexus Pharmaceuticals regarding cyclophosphamide liquid formulations used in cancer treatment.

Dr. Reddy's to Launch Sanofi's Beyfortus in India for RSV Prevention in Infants

Dr. Reddy's Laboratories has secured exclusive rights to promote and distribute Sanofi's novel RSV drug Beyfortus (nirsevimab) in India, expanding their existing vaccine partnership.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.