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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

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

Amiodarone Hydrochloride

Approval Date
Mar 1, 2024
FDA

ERRIN

Approval Date
Mar 1, 2024
FDA

DISOPYRAMIDE PHOSPHATE

Approval Date
Mar 1, 2024
FDA

Famotidine

Approval Date
Feb 22, 2024
FDA

Estazolam

Approval Date
Feb 5, 2024
FDA
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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 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.

FDA Approves 25 First-Time Generic Drugs in First Half of 2025, Expanding Access to Critical Therapies

The FDA approved 25 first-time generic drugs in the first six months of 2025, including generics for critical medications treating HIV, cancer, and neurological conditions.

Real-World Studies Confirm Bevacizumab Biosimilars Deliver Cost Savings and Equivalent Clinical Outcomes in Metastatic Colorectal Cancer

A Canadian population-based study found bevacizumab biosimilars Mvasi and Zirabev provided $6,379 CAD in annual cost savings per patient compared to originator Avastin while maintaining equivalent survival outcomes in metastatic colorectal cancer.

Novo Nordisk Plans India Entry for Ozempic Despite Looming Patent Expiry as Indian Pharma Giants Prepare Generic Alternatives

Danish pharmaceutical giant Novo Nordisk confirms readiness to launch its blockbuster GLP-1 drug Semaglutide (Ozempic) in India despite patent expiration in January 2026, emphasizing continued market leadership strategy.

Rigel Pharmaceuticals Reports Strong Growth with TAVALISSE and REZLIDHIA in 2024, Expands Global Reach

Rigel Pharmaceuticals achieved significant revenue growth in 2024, with TAVALISSE sales increasing 12% to $104.8 million and REZLIDHIA sales growing 118% to $23.0 million.

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