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The document is a letter from the Nonprescription Drug Manufacturers Association (NDMA) to the FDA, expressing concerns about the proposed removal of ephedrine from the OTC monograph due to diversion issues. NDMA argues that legitimate ephedrine products are safe and effective for consumers and that banning them would undermine public health while failing to address illegal drug manufacturing. The letter emphasizes that diversion control should be managed by the DEA, not through FDA's regulatory actions, and requests a public hearing to discuss these issues further.

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