Breckenridge Announces Final Approval Of Its ANDA For Pomalidomide Capsules (Generic For Pomalyst)
Berlin, CT (Press Release) – Breckenridge Pharmaceutical, Inc. announced today that the U.S. Food and Drug Administration has approved Breckenridge's Abbreviated New Drug Application for Pomalidomide Capsules (generic for Pomalyst®).
Breckenridge has partnered with Natco Pharma Limited for the development and manufacture of this product. According to industry sales data, Pomalyst had annual sales of $957 million during the twelve months ending September 2020. Celgene, Breckenridge and Natco have settled the U.S. district court litigation with respect to this product.
About Breckenridge
Breckenridge Pharmaceutical, Inc., a subsidiary of Towa Pharmaceutical (Osaka, Japan), partners with manufacturers nationwide and around the world to bring quality, cost-effective generic pharmaceuticals to U.S. patients. With our dedication to customer service, on-time delivery, reliable supply and quality manufacturing, we improve the health and lives of the patients we and our customers serve.
www.bpirx.com
About Natco
Natco Pharma Limited is global generic pharmaceutical research, development, manufacturing and marketing company. The company was established in 1981 in India. Natco supplies pharmaceutical products to over 50 countries across the globe, including the United States. Natco focuses on the development and manufacturing of oncology and other specialty pharmaceuticals.
*All brand names and trademarks are the property of their respective owners.
Source: Breckenridge Pharmaceutical.
Related Press Releases:
- NATCO Settles Generic Carfilzomib Injection Patent Litigation In The U.S. Market
- Bristol-Myers Squibb Receives Positive CHMP Opinion Recommending Approval Of Empliciti (Elotuzumab) Plus Pomalidomide And Low-Dose Dexamethasone For Treatment Of Patients With Relapsed And Refractory Multiple Myeloma
- European Commission Approves Empliciti (Elotuzumab) Plus Pomalidomide And Low-Dose Dexamethasone (EPd) For The Treatment Of Patients With Relapsed And Refractory Multiple Myeloma
- Genmab Announces European Myeloma Network And Janssen Achieve Positive Topline Results From Phase 3 APOLLO Study Of Daratumumab In Combination With Pomalidomide And Dexamethasone In Relapsed Or Refractory Multiple Myeloma
- Health Canada Approves Pomalyst-Based Triplet Combination For Patients With Multiple Myeloma