Medicaid payment for generic drugs: achieving savings and access.

Christie Provost Peters
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Abstract

Medicaid payment for generic prescription drugs has been a point of contention for the pharmacy industry over the past few years because of reimbursement formula changes contained in the Deficit Reduction Act (DRA) of 2005. The Patient Protection and Affordable Care Act (PPACA) includes provisions to resolve some of these issues. The DRA reduced the maximum amount the federal government would pay state Medicaid programs for generic drugs, and the Centers for Medicare & Medicaid services (CMS) final regulation, to implement the DRA provisions was met with a lawsuit from the pharmacy industry. An injunction by the federal district court, followed by a congressional moratorium, kept CMS from implementing the regulation and kept the pre-DRA formula for the generic drug payment limit in place. PPACA provisions increase maximum federal reimbursement levels for Medicaid generic drugs, but the impact on the pharmacy industry depends on CMS implementation and state policies. This paper examines Medicaid payment for generic drugs, the DRA and PPACA changes to generic drug reimbursement, the concerns of the pharmacy industry, and the potential impact on access.

仿制药的医疗补助支付:实现储蓄和获取。
在过去的几年里,由于2005年赤字削减法案(DRA)中包含的报销公式的变化,非专利处方药的医疗补助支付一直是制药行业争论的焦点。《患者保护和平价医疗法案》(PPACA)包括解决其中一些问题的条款。DRA降低了联邦政府向州医疗补助计划支付仿制药的最高金额,而医疗保险和医疗补助服务中心(CMS)实施DRA条款的最终规定遭到了制药行业的诉讼。联邦地区法院的禁令,随后国会的暂停,阻止了CMS实施该规定,并保留了dra之前的仿制药支付限额公式。PPACA条款提高了医疗补助仿制药的最高联邦报销水平,但对制药行业的影响取决于CMS的实施和各州的政策。本文考察了医疗补助对仿制药的支付、DRA和PPACA对仿制药报销的改变、制药行业的关注以及对可及性的潜在影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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