Except for a drug or device for which the U.S. Food and Drug Administration has issued a black box warning, the Program may not apply a prior authorization requirement for a contraceptive drug or device that is: An intrauterine device; or An implantable rod; Approved by the U.S. Food and Drug Administration; and Obtained under a prescription written by an authorized prescriber. The Program shall provide coverage for a single dispensing to an enrollee of a supply of prescription contraceptives for a 12–month period.