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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 016990
Company: SANOFI AVENTIS US

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
INTAL CROMOLYN SODIUM 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** CAPSULE;INHALATION Discontinued None Yes No
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