HARTFORD, Conn.--(BUSINESS WIRE)-- The United States Food and Drug Administration today announced that specialty pharmacies can continue compounding 17P (hydroxyprogesterone caproate) based on a valid prescription for an individually identified patient.
“Today's FDA decision is an outstanding win for women and their at-risk babies who may have lost access to a safe and cost-effective treatment to help prevent preterm birth. Aetna has championed the need to provide 17P at an affordable price so that pregnant women would not face a 100-fold increase in treatment cost. The FDA's decision is well-reasoned and helps keep quality health care more affordable,” said Lonny Reisman, M.D., Aetna chief medical officer.
Aetna (NYSE: AET) is one of the nation’s leading diversified health care benefits companies, serving approximately 35.3 million people with information and resources to help them make better informed decisions about their health care. Aetna offers a broad range of traditional, voluntary and consumer-directed health insurance products and related services, including medical, pharmacy, dental, behavioral health, group life and disability plans, and medical management capabilities and health care management services for Medicaid plans. Our customers include employer groups, individuals, college students, part-time and hourly workers, health plans, governmental units, government-sponsored plans, labor groups and expatriates. For more information, see www.aetna.com. To learn more about Aetna's innovative online tools, visit www.aetnatools.com.
Tammy Arnold, 713-721-7891
KEYWORDS: United States North America Connecticut
INDUSTRY KEYWORDS: Women Health Pharmaceutical Professional Services Insurance FDA Consumer General Health Managed Care