NEW YORK, August 11, 2017 /PRNewswire/ --
If you want a Stock Review on PCRX, EGRX, NEOS, or ZYNE then come overto http://dailystocktracker.com/register/ and sign up for your free customized report today. Today, DailyStockTracker.com takes note of the most recent performances of Pacira Pharmaceuticals Inc. (NASDAQ: PCRX), Eagle Pharmaceuticals Inc. (NASDAQ:
Parsippany, New Jersey headquartered Pacira Pharmaceuticals Inc.'s stock finished Thursday's session 1.23% lower at $36.20. A total volume of 800,623 shares was traded, which was above their three months average volume of 707,390 shares. The Company's shares have gained 12.07% since the start of this year. The stock is trading below its 200-day moving average by 13.76%. Moreover, shares of Pacira Pharma, which develops, manufactures, and commercializes proprietary pharmaceutical products primarily for use in hospitals and ambulatory surgery centers in the US, have a Relative Strength Index (RSI) of 24.02.
On August 09th, 2017, Pacira Pharma announced that members of its management team are scheduled to present at the 2017 Wedbush Pacgrow Healthcare Conference at 9:10 a.m. ET on August 15th, 2017, in New York City. The live audio webcast of the presentation can be accessed by visiting the "Investors & Media" section of the Company's website. Your complete research report on PCRX can be retrieved for free at:
Shares in Woodcliff Lake, New Jersey headquartered Eagle Pharmaceuticals Inc. rose 1.87%, ending yesterday's session at $50.07. A total volume of 618,359 shares was traded, which was above their three months average volume of 438,900 shares. The stock is trading 28.60% below its 50-day moving average. Moreover, shares of Eagle Pharma, which focuses on developing and commercializing injectable products primarily in the critical care and oncology areas in the US, have an RSI of 28.06.
On July 26th, 2017, Eagle Pharma announced that it has received a Complete Response Letter from the US Food and Drug Administration (FDA) regarding its 505(b)(2) New Drug Application for RYANODEX® (dantrolene sodium) for the treatment of exertional heat stroke (EHS), in conjunction with external cooling methods. In its letter, the FDA has requested that the Company to conduct an additional clinical trial for RYANODEX for EHS.
On July 27th, 2017, research firm RBC Capital Markets reiterated its 'Outperform' rating on the Company's stock with a decrease of the target price from $94 a share to $81 a share. A free report on EGRX is just a click away at:
On Thursday, Grand Prairie, Texas headquartered Neos Therapeutics Inc.'s stock climbed 2.92%, to close the day at $7.05. A total volume of 690,686 shares was traded, which was above their three months average volume of 626,830 shares. The Company's shares have advanced 6.82% in the last one month and 20.51% on an YTD basis. The stock is trading 2.67% above its 200-day moving average. Additionally, shares of Neos Therapeutics, which engages in the development, manufacture, and commercialization of products for the treatment of attention deficit hyperactivity disorder using its drug delivery technologies, have an RSI of 51.59.
On August 08th, 2017, Neos Therapeutics reported financial results for Q2 ended June 30th, 2017. Total product revenues for the quarter were $4.9 million, cost of goods sold was $2.6 million, gross profit was $2.3 million, and net loss was $18.7 million. At June 30th, 2017, the Company held $78.6 million in cash and cash equivalents and short-term investments.
On August 09th, 2017, research firm RBC Capital Markets reiterated its 'Outperform' rating on the Company's stock with a decrease of the target price from $20 a share to $12 a share. Sign up for your complimentary research report on NEOS at:
Shares in Devon, Pennsylvania headquartered Zynerba Pharmaceuticals Inc. ended the day 4.47% lower at $7.26. A total volume of 2.32 million shares was traded, which was above their three months average volume of 678,510 shares. The stock is trading below its 50-day moving average by 57.45%. Furthermore, shares of Zynerba Pharma, which focuses on developing and commercializing proprietary synthetic cannabinoid therapeutics formulated for transdermal delivery, have an RSI of 25.11.
On August 07th, 2017, Zynerba Pharma announced top-line results from its double-blind, placebo-controlled Phase-2 STAR 1 clinical trial evaluating ZYN002 (cannabidiol [CBD] gel) in adult epilepsy patients with focal seizures. ZYN002 did not demonstrate a statistically significant reduction of focal seizures during the treatment period compared to the baseline period for either the high- or low-dose cohorts compared to placebo. Register for free on DailyStockTracker.com and download the latest research report on ZYNE at:
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