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FDA Hits Marketing Of Unapproved Codeine Sulfate Tablets

Four companies required to stop making and distributing illegal pain relievers

By James Limbach
ConsumerAffairs.com

October 13, 2009->
The Food and Drug Administration has told four companies that they must stop marketing unapproved codeine sulfate tablets. These drugs are opioid analgesics -- commonly called narcotics -- that are widely used to treat pain.

These particular products have not received FDA approval and the agency says it has no evidence that they are safe and effective. Another manufacturer, Roxane Laboratories, markets FDA-approved codeine sulfate tablets and is able to meet the demand for the drug.

The FDA says it does not anticipate a supply problem for codeine sulfate tablets.

"Consumers deserve and expect that their drugs meet modern FDA standards for safety, effectiveness, labeling, and quality. Removing unapproved products that do not meet those standards is an FDA priority," said Janet Woodcock, M.D., director of the FDA's Center for Drug Evaluation and Research (CDER). "The FDA urges drug companies to ensure all drugs they make and market have appropriate FDA approval."

The names of the products and the manufacturers and distributors that received the warning letters are:

• Codeine Sulfate Tablets, 30 mg, 60 mg -- Lehigh Valley Technologies Inc., Allentown, Penn.

• Codeine Sulfate Tablets, 30 mg, 60 mg -- Cerovene Inc., Valley Cottage, N.Y.

• Codeine Sulfate Tablets, 30 mg -- Dava International Inc., Fort Lee, N.J.

• Codeine Sulfate Tablets, 30 mg, 60 mg -- Glenmark Generics Inc. USA, Mahwah, N.J.

Companies receiving the warning letters have 15 days to give the FDA a plan to discontinue marketing the unapproved drugs. Manufacturers have 90 days to cease manufacturing of new product, and distributors have 180 days to cease further shipment of existing products. Previously manufactured unapproved products may still be found on pharmacy shelves for a period of time.

"Doctors and patients often find that some drugs on the market do not have FDA approval," said Deborah M. Autor, director of CDER's Office of Compliance. "This lack of approval undermines the FDA's process to ensure that safe and effective drugs are available to the U.S. public."

Consumers who rely on opioid analgesics for pain relief have access to products that have been evaluated by the FDA and determined to be safe and effective for use. There are other FDA-approved drugs, including different opioid analgesics, which can be used to relieve pain. Consumers should consult a health care professional for detailed guidance on treatment options.

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