Pharmaceutical Outsourcing covers news of importance to the contract services segment of the pharmaceutical industry.
Collected from the most trusted on-line resources, these news stories are chosen and published here based on their relevance to the pharmaceutical industry.
Topics of interest typically include: mergers and acquisitions, service additions, new capabilities, personnel changes, news from the FDA and other international regulatory and standard-setting agencies, and new outsourcing contracts and deals.
If you are looking to stay up-to-date with the news in your industry, this resource is vital for your industry knowledge.
Wednesday, October 10, 2018
Dr. Reddy’s Laboratories has launched Colesevelam HCl Tablets, USP, a therapeutic equivalent generic version of WELCHOL in the United States market approved by the FDA.
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Monday, December 30, 2019
Dr. Reddy’s announced the launch of Sodium Nitroprusside Injection, 50 mg/2 mL (25 mg/mL) Single-dose Vial, the therapeutic generic equivalent of Nitropress® Injection.
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Dr. Reddy’s announced the launch of Ziprasidone Mesylate for Injection, 20 mg (base)/mL Single-dose Vials, the generic equivalent of Geodon.
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Dr. Reddy’s and its subsidiary, Promius Pharma announced the filing of NDA for its migraine candidate DFN-02 with the FDA.
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Dr. Reddy’s Laboratories has announced the acquisition of a portfolio of over-the-counter (OTC) brands in the cough-and-cold, pain, and dermatology categories. The company acquired six OTC brands from Ducere Pharma, including DOAN’S®, BUFFERIN®, ...
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Dr. Reddy's Laboratories Limited and Integra LifeSciences Holdings Corporation have entered into an exclusive distribution agreement. Under the agreement, Dr. Reddy’s will market and distribute DuraGen Plus® and Suturable DuraGen® Dural Regeneration ...
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Dr. Reddy’s has entered into a purchase agreement with Upsher-Smith Laboratories, pursuant to which the company would sell its US and select territory rights for ZEMBRACE®, SYMTOUCH®, and TOSYMRA™.
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Wednesday, October 23, 2019
Dr. Reddy’s confirms it initiated a voluntary nationwide recall of all of its ranitidine medications sold in US due to confirmed contamination with NDMA above levels established by the FDA.
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Dr. Reddy's Laboratories and XenoPort have entered into a license agreement pursuant to which Dr. Reddy’s Laboratories will be granted exclusive U.S. rights for the development and commercialization of XenoPort’s clinical-stage oral new chemical ...
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Monday, February 01, 2016
Dr. Reddy's Laboratories has announcedthat the U.S. Food and Drug Administration tentative approval for Zenavod™ (doxycycline) Capsules, 40 mg. Zenavod is a tetracycline-class drug indicated for the treatment of only inflammatory lesions (papules and...
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Dr. Reddy’s announced the launch of Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg Extended-Release Tablets, USP.
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Wednesday, December 20, 2017
The US subsidiary of Dr. Reddy’s has reached a settlement with the US Government involving packaging for five blister-packed prescription products.
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Wednesday, February 19, 2020
Dr. Reddy’s Laboratories has entered into a definitive agreement with Wockhardt Limited to acquire select divisions of its branded generics business.
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Dr. Reddy’s Laboratories and CHD Bioscience announced a global licensing agreement for the clinical development and commercialization of Dr. Reddy’s Phase III clinical trial candidate, DFA-02.
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Dr. Vince Clinical Research (DVCR), a full-service contract research organization (CRO), announced the appointment of Sheldon Preskorn, M.D., as its Senior Vice President of Neuroscience.
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