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Stock Market & Financial Investment News

News Breaks
June 20, 2014
11:29 EDTACT, AKRXFTC approves settlement with Akorn over Hi-Tech Pharmacal acquisition
The Federal Trade Commission has approved a final order settling charges that Akorn Enterprises’ (AKRX) $640M acquisition of Hi-Tech Pharmacal was anticompetitive and would lead to higher prices for consumers in several current and future generic drug markets. The final order settling the FTC’s charges requires the parties to sell either Akorn’s or Hi-Tech’s rights and assets to each of five drug products to Watson Laboratories (ACT) and required Akorn to assign Watson its contract for making a currently available branded and generic topical anesthetic cream within 10 days after the deal is completed. Reference Link
News For AKRX;ACT From The Last 14 Days
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April 15, 2015
10:00 EDTAKRXOn The Fly: Analyst Initiation Summary
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09:02 EDTAKRXRBC sees Akorn as possible play on Perrigo takeover interest
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08:19 EDTAKRXAkorn management to meet with Deutsche Bank
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06:24 EDTAKRXAkorn initiated with an Overweight, $61 target at JPMorgan
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April 14, 2015
06:18 EDTACTActavis urges U.S. appeals court to reverse decision on Namenda, AP reports
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April 13, 2015
16:37 EDTACTActavis announces availability of 52mg Liletta to prevent pregnancy
Actavis and Medicines360, a nonprofit women's health pharmaceutical company, announced that Liletta 52 mg is now available in the U.S. for use by women to prevent pregnancy for up to three years.
10:52 EDTACTMeister says Actavis bought great companies, can continue growing
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09:27 EDTACTActavis and Medicine360 announce Liletta es available in the U.S.
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08:34 EDTACTZoetis names Actavis Executive Chairman Paul Bisaro to board
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April 9, 2015
11:39 EDTACTPershing Square, Valeant, Allergan drop lawsuit over buyout
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April 8, 2015
12:17 EDTAKRXOn The Fly: Midday Wrap
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11:35 EDTAKRXGeneric drug maker Akorn up 4% to $49.80 after Myla offers to buy Perrigo
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11:34 EDTAKRXGeneric drug maker Akorn up 4% to $49.80 after Myla offers to buy Perrigo
09:16 EDTACTActavis COPD drug Daliresp gets Paragraph 4 challenge
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08:05 EDTACTActavis price target raised to $348 from $328 at Leerink
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08:04 EDTACTActavis potential acquisition Rhythm initiates Phase 2b study of relamorelin
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07:34 EDTACTActavis initiates Phase 2b clinical trial of relamorelin
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April 7, 2015
14:23 EDTAKRXAkorn initiated with a Buy at Deutsche Bank
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April 5, 2015
14:43 EDTACTActavis seeks FDA approval to market generic version of Gilead's Letairis
Actavis (ACT) on Friday, confirmed that it has filed an Abbreviated New Drug Application with the FDA seeking approval to market Ambrisentan Tablets, 5 mg and 10 mg. Actavis' ANDA product is a generic version of Gilead Science's (GILD) Letairis, which is a treatment for pulmonary arterial hypertension. Gilead Sciences and Royalty Pharma Collection Trust filed suit against Actavis on April 1, in the U.S. District Court for the District of Delaware seeking to prevent Actavis from commercializing its ANDA product prior to the expiration of U.S. Patent number RE42,462. The lawsuit was filed under the provisions of the Hatch-Waxman Act, resulting in a stay of final FDA approval of Actavis' ANDA for up to 30 months from the date the plaintiffs received notice of Actavis' ANDA filing or until final resolution of the matter before the court, whichever occurs sooner, subject to any other exclusivities. Based on available information, Actavis believes it may be a "first applicant" to file an ANDA for the generic version of Letairis and, should its ANDA be approved, may be entitled to 180 days of generic market exclusivity. For the 12 months ending December 31, Letairis had global sales of approximately $595M, according to Gilead.

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