Quantcast

Latest Breckenridge Pharmaceutical Inc. Stories

2011-06-10 11:22:00

BOCA RATON, Fla., June 10, 2011 /PRNewswire/ -- Breckenridge Pharmaceutical, Inc. announced today that the U.S. Food and Drug Administration has granted final approval for the Company's Abbreviated New Drug Application (ANDA) to market its generic version of Activella® 0.5mg/0.1mg Tablets. The company currently markets an equivalent to Activella® 1.0mg/0.5mg Tablets, as (Estradiol/Norethindrone Acetate 1.0mg/0.5mg) Tablets. Estradiol/Norethindrone...

2011-06-10 10:51:00

BOCA RATON, Fla., June 10, 2011 /PRNewswire/ -- Breckenridge Pharmaceutical, Inc. announced today the immediate launch of Letrozole 2.5 mg Tablets. The U.S. Food and Drug Administration granted final approval for the Abbreviated New Drug Application (ANDA) for this product, which is being supplied under a licensing agreement. Letrozole Tablets are AB rated to Femara®, a $700 million dollar oncology drug marketed by Novartis. About Breckenridge: Breckenridge...

2011-05-16 10:43:00

BOCA RATON, Fla., May 16, 2011 /PRNewswire/ -- Breckenridge Pharmaceutical, Inc. announced that Breckenridge and Synthon Pharmaceuticals, Inc. have reached an agreement with Takeda Pharmaceutical Company Limited and Takeda Pharmaceuticals North America resolving patent litigation related to Pioglitazone Hydrochloride 15 mg, 30 mg and 45 mg tablets, a generic equivalent version of Actos®. Under the terms of the agreement, Takeda granted Breckenridge and Synthon a...

2011-04-04 13:03:00

BOCA RATON, Fla., April 4, 2011 /PRNewswire/ -- Breckenridge is announcing that it entered into an agreement with Oman Pharmaceutical Products Company LLC, of Salalah, Sultanate of Oman to market Neomycin Sulfate Tablets. Under the terms of the agreement, the product will be manufactured by Oman Pharma, and marketed and distributed by Breckenridge on an exclusive basis in the United States. The ANDA has been approved by the U.S. Food and Drug Administration (FDA), and the companies began...

2010-07-28 11:00:00

BOCA RATON, Fla., July 28 /PRNewswire/ -- Breckenridge announced today that through its agreement with Tris Pharma, the company will market Methylphenidate Solution, the generic version of Methylin® marketed by Shionogi Pharma, Inc., under an Abbreviated New Drug Application (ANDA). Under the terms of this agreement, the products will be manufactured by Tris Pharma, and marketed and distributed by Breckenridge on an exclusive basis in the U.S. The companies plan to start...

2010-06-28 18:15:00

BOCA RATON, Fla., June 28 /PRNewswire/ -- Breckenridge Pharmaceutical, Inc. announced today that they will launch Anastrozole 1mg Tablets. The U.S. Food and Drug Administration has granted final approval for the Abbreviated New Drug Application (ANDA) for this first time generic, which is being supplied under a licensing agreement. Anastrozole Tablets are AB rated to Arimidex®, a billion dollar cancer drug marketed by AstraZeneca. Breckenridge will launch the product...

2010-06-09 16:16:00

BOCA RATON, Fla., June 9 /PRNewswire/ -- Breckenridge Pharmaceutical, Inc. announced today that the U.S. Food and Drug Administration has granted final approval for the Company's Abbreviated New Drug Application (ANDA) for Terbinafine HCl Tablets, 250mg. Terbinafine HCl Tablets are AB rated to Lamisil®, a brand product marketed by Novartis. Breckenridge plans to launch the product this summer. About Breckenridge: Breckenridge Pharmaceutical is a privately held...

2009-11-10 11:10:00

BOCA RATON, Fla., Nov. 10 /PRNewswire/ -- Breckenridge announced today that it has entered into an agreement with Genepharm to commercialize two ANDA's for two separate cancer drugs with combined U.S. branded sales of approximately $1.7 billion. Under the terms of this agreement, the products will be marketed and distributed by Breckenridge and will be supplied by Genepharm. One product has received a pre approval and will be launched upon patent expiration. The second product is...

2009-08-17 14:52:00

BOCA RATON, Fla., Aug. 17 /PRNewswire/ -- Breckenridge announced today that it has entered into an agreement with Orit Laboratories to market the Company's Abbreviated New Drug Application (ANDA) for Ergocalciferol Capsules, USP, 50,000 USP Units (1.25mg), (Vitamin D), the generic version of Drisdol(R) by Sanofi-aventis. The product was approved by the U.S. Food and Drug Administration (FDA) on May 20, 2009. Under the terms of this agreement the product will be supplied by Orit...


Word of the Day
reremouse
  • A bat.
The word 'reremouse' comes from Middle English reremous, from Old English hrēremūs, hrērmūs ("bat"), equivalent to rear (“to move, shake, stir”) +‎ mouse.
Related