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On August 8, 2001, we received FDA approval for our Abbreviated New Drug Application (ANDA) for sales of isosorbide mononitrate extended-release tablets in 30 mg and 120 mg strengths. L) received approval for its Abbreviated New Drug Application (ANDA) for sales of isosorbide mononitrate extended-release tablets in 30 mg and 120 mg strengths from the United States Food and Drug Administration (FDA). IVAX Corporation (AMEX:IVX) today announced that the United States Food and Drug Administration (FDA) has approved its Abbreviated New Drug Application (ANDA) for isosorbide mononitrate extended-release 60 mg tablets. |
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