The brand-name manufacturer thus does not solicit or encourage duplication of its products or labeling, but the generic manufacturer does not unilaterally or unexpectedly choose to imitate the brand-name manufacturer’s actions. The imitation of the brand-name products is systematic and overseen by the FDA, making it not only highly foreseeable to the brand-name manufacturer but also effectively subject to the brand-name manufacturer’s control. If the generic drug is an insufficiently close copy of the brand-name product, for example, the brand-name manufacturer can have the FDA remove the generic drug from the market.252 Likewise, if the brand-name manufacturer determines that the product’s warnings or instructions should be enhanced in some way, the FDA will force generic producers of the drug to fall perfectly in line behind the brand-name manufacturer’s lead.253 The unique regulatory scheme surrounding prescription drugs thus provides a mechanism by which the copying of brand-name drugs’ designs and labeling is not initiated or encouraged by the brand-name manufacturer, but it is nevertheless systematic, predictable, and subject to significant control by the brand-name manufacturer through the FDA.