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Prices of generic cymbalta, mibolerone, and topiramate - the amount of amitriptyline prescribed to children and adolescents by U.S. prescribers per 100 patients - the amount of benzodiazepines prescribed to children and adolescents by U.S. prescribers per 100 patients - the average daily dose for methylphenidate (Ritalin) prescriptions in the U.S. per 100 children and adolescents, as published by the Food and Drug Administration - the average daily dose for lisdexamfetamine dimesylate lisinopril retail cost in the U.S. per 100 children and adolescents, as published by the Food and Drug Administration - the amount of prescription painkiller tramadol prescribed in the U.S. per 100 children and adolescents year, what is the cost of lisinopril without insurance for both children and Is there a generic for lisinopril adolescents aged 6 or older - the amount of diclofenac (Voltaren) in the U.S. prescribed to children and adolescents per 100 - the amount of hydrocodone prescribed to children and adolescents per 100 - the amount of ibuprofen prescribed in the U.S. per 100 children and adolescents - the amount of codeine prescribed in the U.S. per 100 children and adolescents. In its report on the prescription drugs, FDA stated in its comments that the company failed to provide a "comprehensive and correct list of all information it has on its database," such as the cost of prescription drugs. The FDA noted that company "failed to adequately document the effectiveness of its database. FDA reviewed pharmacy data and concluded that the company's methodology for estimating its database cost is likely to create serious overpayment of such costs. FDA also raised concerns about the effectiveness of its database as it did not include all the drugs available or generic copies to the U.S. market." However the New York Times, in its report on the settlement, noted that "The Justice Department did not file a written statement" but instead issued a two-page statement "on its own, which was distributed to some of the companies." statement made numerous references to how the department "takes seriously its commitment to consumer protection." The New York Times also reports "that the Justice Department's agreement not to appeal the case is first time it has declined to pursue a case for antitrust violations in the drug marketing business." New York Times In a separate investigation of the industry, AP reported on November 1, 2011 that: The Justice Department is investigating drug companies over allegations that they have pushed on too many patients for drugs that do more harm than good and should not be prescribed, according to officials familiar with the probes. The investigations involve several companies, but the AP has learned one of the biggest is Cephalon, which treats conditions including cystic fibrosis and multiple sclerosis. The Justice Department is seeking documents from Cephalon and other drug companies as part of its inquiry into alleged over-prescribing for chronic conditions such as high blood pressure, cholesterol, diabetes, and obesity. The investigations are being conducted in cooperation with the Federal Trade Commission and state attorneys general, the officials said. A spokesman for the company, Joseph H. Martin, would not comment beyond a prepared statement: "This matter is still in an early phase of the department's review. Given that this is an ongoing legal investigation, it would be inappropriate and we have no additional details to share at this time." In an earlier statement, Martin indicated Cephalon was cooperating with the government. "We are aware of the ongoing investigations by Justice Department and others, believe the information collected will identify areas of improvement in patient access to prescription drugs," Martin said in the statement.

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