The Company has entered into several alliance, collaboration, license and distribution agreements, and similar agreements with respect to certain of its products and services, with unrelated third-party pharmaceutical companies. How do I let you know of a change of address? The dividend yield of zero is based on the fact that the Company has never paid cash dividends on its common stock, and has no present intention to pay cash dividends. The fair value was determined by a model-derived valuation utilizing Level 2 inputs which are observable or whose significant value drivers are observable. The Company records the alliance agreement partner's adjustments to such estimated amounts in the period the agreement partner reports the amounts to the Company. Share-based compensation expense. The Barclays Credit Agreement was subsequently terminated in accordance with its terms on June 30, after the Company used a portion of the proceeds from its offering of the 2. This derivative liability will be remeasured at fair value at each reporting period, and changes in fair value will be reflected in current period earnings, as appropriate. Research and development. I began to respond N but as I pressed send I was informed that this would incur charges so I stopped in case it was a scam.
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Intangible assets, net.
Inventory, net of carrying value reserves at June 30, and December 31, consisted of the following:. Level 1. Options exercisable at September 30, Total share-based compensation expense recognized in the consolidated statements of operations during the three and six month periods ended June 30, and was as follows:.
is a legitimate Barclays number (as is ) and, ironically, is used to Barclays Bank customer service number: + I've had a text from supposedly from Barclays asking me if I had authorised a I don't have a bank account with Barclays, only a small credit card.
Googled the number as it seemed strange. Generally it takes one to three years after an application for a new indication is submitted to obtain approval from the applicable regulatory agency.
Total intangible assets.
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Although the Supply Term expired on September 30,the Company is permitted to sell any AG Products in its inventory or owed to the Company by Shire under the Amended and Restated Shire Agreement until all such products are sold; the Company will pay a profit share to Shire on sales of such products. This hierarchy maximizes the use of observable inputs and minimizes the use of unobservable inputs.
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Payroll-related expenses. The Company is required to pay a profit share to Tolmar on sales of each product commercialized pursuant to the terms of the Tolmar Agreement.
Impax Specialty Pharma is engaged in the development of proprietary brand pharmaceutical products that the Company believes represent improvements to already-approved pharmaceutical products addressing CNS disorders and other select specialty segments. June 30, The Company will sell its manufactured branded product to customers in the ordinary course of business through Impax Specialty Pharma.
Tower currently marketed products. The Company has entered into several alliance, collaboration, license and distribution agreements, and similar agreements with respect to certain of its products and services, with unrelated third-party pharmaceutical companies.
GRIEBENSCHMALZ HALTBARKEIT MEANING
|Under the Amended and Restated Development Agreement, RiconPharma is responsible for exclusively developing and manufacturing, on a non-exclusive basis, for the Company and the Company is responsible for commercializing Griseofulvin Ultra-microcrystalline mg and mg tablets.
As the private offering closed on the last day of the quarter ended June 30,there was no related interest expense recorded for the second quarter, and there was no accrued interest payable balance on the Notes as of June 30, I mpax Laboratories, Inc.
Under the terms of the Tolmar Agreement, Tolmar granted to the Company an exclusive license to commercialize up to 11 generic topical prescription drug products, including ten currently approved products and one product pending approval at the FDA, in the United States and its territories.
The Company will be responsible for conducting clinical studies and preparing regulatory filings related to the development of any such additional products and would bear all related costs. In exchange for these deliverables, the Company receives payments from its agreement partners for product shipments and research and development services, and may also receive other payments including royalty, profit sharing, upfront, and periodic milestone payments.
The Company also considers other factors, including significant market changes which may impact future expected returns, and actual product returns.