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WASHINGTON, April 17 () -- The U.S. Food and Drug Administration said generic drug companies may not produce the patent-expired version OxyContin due to its use as a street drug.The decision could be considered groundbreaking since it is the first time the FDA has ruled a tamper-resistant version of a narcotic drug trumped the health benefits of a cheaper product that more patients could afford, the FDA's Dr. Douglas Throckmorton said.Had the FDA approved the production of a generic OxyContin, it would have been allowing companies to produce a drug with a decade-long track record of abuse.OxyContin was first produced in 1995 by Purdue Pharma under the expectation its time-release properties would make it safe.But it was quickly discovered that crushing the pill allowed abusers several choices for ingestion that were dangerous and addicting,[url=http://www.isabelmarantsneakersbootss.com/]isabel marant boots[/url], The New York Times reported Wednesday.Purdue then developed a form of the pill that turns into a jelly-like goo when crushed. But that gave rise to accusations drug companies will wait until the last minute to introduce tamper-proof versions of their blockbuster drugs to extend their monopolies.The patent for OxyContin in its original form expired Tuesday. The patent for the tamper-proof version does not expire until 2025.