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The Food and Drug Administration has ordered that Pfizer Inc. and its subsidiaries, including the generics company, Teva Pharmaceutical Industries Ltd., and the other companies, which manufacture, market and sell the generic versions of the erectile dysfunction drug Viagra, be required to pay as much as $50 million for each of the three generic products, according to a release issued by its website on Monday.

The three generic versions of the drug are generic versions of sildenafil, the generic version of Viagra, and diflucan, a combination of the two.

The agency's order is based on a review of the documents filed in the FDA's Office of Generic Drugs, which are available at.

Pfizer and Teva also will be required to pay an additional $30 million to resolve the complaints filed against them, the company said. These were based on complaints filed in the FDA's Office of Generic Drugs, which is available at.

The company said that its research team had evaluated the generics of Viagra, sildenafil and diflucan, as well as those of the other three generic products. The company has not given an explanation for the amount of money the agency is requesting.

The company did not provide any details about the three generic drugs, as the FDA said that it does not regulate the use of generic drugs, although the agency's research team and other regulatory agencies have said that the companies' patents were valid and infringed on Pfizer's patents. Pfizer has not confirmed that it is aware of any patent infringement or that the three generics products are not approved by the FDA.

The FDA has requested that the company pay $50 million in cash payments to the two generic manufacturers, Teva Pharmaceutical Industries Ltd. and Pfizer Inc., according to its release.

The company also is requesting that Teva pay a separate $15 million royalty to the other three generic manufacturers, Teva Pharmaceutical Industries Ltd. and Pfizer Inc. and the other companies, for each of the three generics.

The FDA is the third to issue a drug safety warning to the companies, which in 2011 began manufacturing and marketing generic versions of the erectile dysfunction drug Viagra. Last year, the agency issued an order to all companies that manufacture the products to take legal action against them.

The agency has also requested that the companies pay an additional $30 million to resolve complaints about the three generic products, according to.

The FDA has also been asked to report any adverse events that have been reported to the agency with respect to the three generic products. The agency has also asked the company to report information that could potentially influence its sales, and the company also has a request to share the information with the FDA, the FDA said.

In a statement, Pfizer said that it has received multiple inquiries from various sources to comment on the information provided. It also said that it has not given an explanation for the amount of money the agency is requesting.

The company said that it has received complaints from the public and health professionals that it has been unable to provide information that could influence the FDA's decision to issue the warnings. It also said that its research team had evaluated the generics of Viagra, sildenafil and diflucan, as well as those of the other three generic products.

The agency has also requested that Teva pay a separate $15 million royalty to the other three generic manufacturers, Teva Pharmaceutical Industries Ltd. and Pfizer Inc., for each of the three generics, and the other companies, for each of the three generic products.

Pfizer has said that it will not be required to pay the $30 million of cash payments the company is requesting as it is a separate company.

In the same release, Pfizer said that the company will also be required to pay $15 million to resolve complaints regarding the three generic products, the FDA said.

The FDA also said that its research team has evaluated the generics of Viagra, sildenafil and diflucan, as well as those of the other three generic products.

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A British company that makes Viagra in the European market was seized by police in a raid at a drug storage facility in the southern island of Cyprus. The operation involved more than 100 staff, most of whom were employed by the pharmaceutical giant AstraZeneca.

The shipment of the anti-impotency drug was seized in the first phase of the operation which involved more than 100 staff, most of whom were employed by AstraZeneca, the company which owns the rights to the drug.

The seizure of the anti-impotency product involved more than 100 staff, most of whom were employed by the pharmaceutical giant AstraZeneca and its partner AstraZeneca, the manufacturer of the drug.

The company said: "The seizure of the anti-impotency drug is one of the largest and most comprehensive seizures of any pharmaceutical company since the early 1980s. We have inspected all the facilities, from storage to storage, and have inspected more than 300,000 packages of drugs in the EU, with almost half of those that are registered in the UK. The product was discovered when the UK Customs officers were searching for the drug on the island of Cyprus.

"The seizures were conducted under close supervision by a team of our officers and specialists, led by the chief executive officer, Dr. Michael Murray. We have inspected all the facilities, from storage to storage, and have inspected more than 300,000 packages of drugs in the EU, with almost half of those that are registered in the UK."

A spokesman for AstraZeneca said: "The seizure of the anti-impotency product is one of the largest and most comprehensive seizures of any pharmaceutical company since the early 1980s."

The company said the UK had supplied about 100,000 packs of the drug to the US. AstraZeneca said the company had "stoked up" the supply to ensure "the safety and effectiveness of the product."

The company added: "We have inspected all the facilities in Cyprus, from storage to storage and have inspected more than 300,000 packages of drugs in the EU, with almost half of those that are registered in the UK."

AstraZeneca said the company had "stoked up" the supply of the drug to ensure "the safety and effectiveness of the product."

The company said the UK had supplied about 100,000 packs of the drug to the US and "the supply was supplied on a contingency basis."

The company said the supply was "not in line with the international supply order", and had "not been made with a guarantee of safety and effectiveness".

AstraZeneca said the company had "stoked up" the supply of the anti-impotency product to ensure "the safety and effectiveness of the product".

The British company, based in London, said: "The UK has supplied about 100,000 packs of the drug to the US and in the supply it was supplied on a contingency basis."

The British company, based in Cambridge, said the company had "stoked up" the supply to ensure "the safety and effectiveness of the product".

AstraZeneca said the company had "stoked up" the supply to ensure "the safety and effectiveness of the product".

The company said the company had "stoked up" the supply of the anti-impotency product to ensure "the safety and effectiveness of the product".

AstraZeneca said the company had "stablished a strong commitment to the safety and effectiveness of the product".

The British company, based in London, said the company had "stablished a strong commitment to the safety and effectiveness of the product".

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