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Aggrenox authorized generic producers to carry out the policy, in accordance with standards established by the Food and Drugs Act (GDR) as deemed appropriate. For further communication, please contact: Kenny D. Burris, Ph.D. Senior Science Policy Analyst National Drug and Therapeutics Information Center Telephone: 609-292-5055 Fax: 608-942-2042 Email: kenny.dubois@druginfoia.usda.gov www.druginfoia.usda.gov/policy Nondrug User Subscribers Druginfoia, a Division of the Drug Enforcement Administration, is responsible for oversight of DEA-registered drug-related activities conducted under the authority of Section 13 GDR. Druginfoia conducts its drug-related activities through a multidiscipline staff that monitors and interprets laws, regulations, policies, guidelines to ensure compliance with all requirements. Druginfoia staff reviews and maintains the files records of registered drug dealers, wholesalers, pharmacy technicians, manufacturers, and manufacturers in compliance with applicable laws and policies. Druginfoia is also responsible for the monitoring and recording of any narcotic drug transactions involving smugglers who are not registered DEA agents. Druginfoia staff periodically review these data to assure compliance with federal drug policy, federal, state and local laws, other relevant federal statutes and to improve record keeping. Druginfoia also maintains a database of registered users and wholesalers where applicable. Druginfoia has taken numerous actions to safeguard registered users and wholesalers, including: - Applying the most stringent record keeping and reporting requirements to ensure their compliance with the Federal laws and regulations; - Adopting Aggrenox 1mg $47.17 - $0.52 Per pill a written recordkeeping procedure with regular audits conducted to ensure that all recordkeeping is current; - Establishing regular and is generic aggrenox available continuous compliance reviews with each registered user and retailer when a case of suspected illegal drug manufacture or distribution is identified Registered users and wholesalers are required to file a quarterly report regarding their activities with Druginfoia, detailing the sale quantities and drug names consumed. Druginfoia its staff will take necessary disciplinary measures against anyone who violates these records requirements. This report also serves as evidence in any civil litigation where evidence is required, to prove certain facts. Drug Dealer Section 13 of the GDR was enacted pursuant to the GDR Customs Act (GDDPA). Druginfoia staff is responsible for administering the GDDPA through oversight and reporting. Druginfoia's policy is designed to ensure the proper handling of illegal drug goods brought into, or transferred out of, the country by druggists, pharmacies, wholesalers, and other persons who handle such goods by, or at their direction, whether authorized or not.

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