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Stock Market & Financial Investment News

News Breaks
May 13, 2014
14:35 EDTACT, MNKActavis' generic version of Exalgo approved by FDA
The FDA approved Actavis’ (ACT) generic version of hydromorphone hydrochloride in strengths of 8 mg, 12 mg and 16 mg on May 12, according to a post to the FDA website. Hydromorphone hydrochloride is sold in branded form under the name Exalgo by Mallinckrodt (MNK). Reference Link
News For MNK;ACT From The Last 14 Days
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November 17, 2014
09:16 EDTACTActavis confirms deal to acquire Allergan for $219 in cash, stock
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09:15 EDTACTActavis confirms deal to acquire Allergan for $219 in cash and shares
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09:10 EDTACTActavis buying Allergan for $219 per share, CNBC reports
08:02 EDTACTActavis completes Durata Therapeutics tender offer
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06:05 EDTACTActavis close to buying Allergan for over $64B, Bloomberg reports
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November 16, 2014
14:02 EDTACTAllergan, Actavis move closer to deal, WSJ reports
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November 14, 2014
17:27 EDTMNKPaulson & Co. gives quarterly update on stakes
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16:58 EDTACTThird Point gives quarterly update on stakes
NEW STAKES: Alibaba (BABA), eBay (EBAY), Bed Bath & Beyond (BBBY), Shire (SHPG), and Parker Hannifin (PH). INCREASED STAKES: Actavis (ACT), Amgen (AMGN), EQT (EQT), Sensata (ST), Coca-Cola Enterprises (CCE). DECREASED STAKES: Williams Cos (WMB), Ally Financial (ALLY), Cheniere Energy (LNG), YPF (YPF), and FedEx (FDX). LIQUIDATED STAKES: AIG (AIG), T-Mobile (TMUS), Rackspace (RAX), Hertz (HTZ), and Citrix Systems (CTXS).
12:53 EDTACTOmega Advisors gives quarterly update on stakes
NEW STAKES: AerCap Holdings (AER), Nordic American Offshore (NAO), Melco Crown Entertainment (MPEL), Groupon (GRPN), and Ashland (ASH). INCREASED STAKES: QEP Resources (QEP), United Continental (UAL), Cabot Oil & Gas (COG), Actavis (ACT), and KAR Auction Services (KAR). DECREASED STAKES: Sprint (S), SandRidge Energy (SD), Sirius XM Holdings (SIRI), Kinder Morgan (KMI), and Transocean (RIG). LIQUIDATED STAKES: QUALCOMM (QCOM), Ocwen Financial (OCN), Freeport-McMoRan (FCX), Boston Scientific (BSX), and Capital One (COF).
09:51 EDTMNKMallinckrodt management to meet with Oppenheimer
Meeting to be held in Europe on November 20 hosted by Oppenheimer.
07:32 EDTACTHayman Capital gives quarterly update on stakes
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November 13, 2014
10:44 EDTMNK, ACTMallinckrodt news on generic Concerta positive for Actavis, says BMO Capital
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08:20 EDTMNKMallinckrodt could be down $6-$8 on FDA reclassification, says UBS
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08:15 EDTACTActavis' sNDA for bipolar disorder candidate Saphris accepted by FDA
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07:23 EDTACTValeant wooing doctors ahead of hoped for Allergan acquisition, WSJ says
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06:11 EDTMNKMallinckrodt responds to FDA expected reclassification of methylphenidate ER
Mallinckrodt has been informed by the FDA that the agency has reason to believe that the company’s methylphenidate hydrochloride extended-release, or ER, tablets, USP may not be therapeutically equivalent to the category reference drug Concerta. As a result, the agency indicated that it has reclassified Mallinckrodt’s ANDA 202608 for methylphenidate ER dosage strengths of 27mg, 36 mg and 54 mg from AB to BX. The agency said that this change was based on the application of its new Draft Guidance for determining bioequivalence of methylphenidate hydrochloride products just published on November 6, 2014. Although the Draft Guidance has an open comment period through January 5, 2015, the agency nevertheless confirmed that this change would be reflected on November 13, 2014 in the on-line Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations. Mallinckrodt strongly believes its methylphenidate ER products are safe and effective when used in accordance with the approved labels. Mark Trudeau, president and CEO of Mallinckrodt stated, “We believe that the FDA’s actions are not supported by sound scientific evidence and not consistent with the best interests of patients." Mallinckrodt methylphenidate ER products have consistently met all quality specifications and the regulatory requirements originally defined by the FDA, and in the 21 months since launch more than 88M doses of these products have been prescribed. In that time, and across all of those patient exposures, the company has received only 68 confirmed adverse events related to a lack of efficacy when the patient switched from the reference listed drug to the company’s methylphenidate ER products.
November 12, 2014
10:09 EDTACTActavis in talks to buy Allergan for over $200 per share, Bloomberg says
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10:01 EDTACTActavis in talks to buy Allergan for $60B, more than $200/share Bloomberg says
Actavis (ACT) is said to seek to pay about $200 per share, but Allergan (AGN) seeks about $210 per share, according to Bloomberg.
November 11, 2014
08:32 EDTACTValeant likely to raise offer for Allergan again, says Bernstein
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November 10, 2014
16:34 EDTACTActavis appoints Maria Teresa Hilado as CFO
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