Document hub

Our international presence

Return to Hikma.com
Contact Us

Popular searches

Hikma receives FDA approval for Rifampin Injection

London, 9 March 2016 – Hikma Pharmaceuticals PLC (“Hikma”) (LSE: HIK) (NASDAQ Dubai: HIK) (OTC: HKMPY), (rated Ba1 Moody’s / BB+ S&P, both stable), the fast growing multinational pharmaceutical group, announces that its abbreviated new drug application (“ANDA”) for Rifampin Injection USP, 600mg/vial has been approved by the U.S. Food and Drug Administration (“FDA”)

Press Release Product 9 March 2016

Rifampin Injection is an anti-infective indicated to treat certain infections such as tuberculosis and leprosy. According to IMS Health, sales of Rifampin Injection in the US market were approximately $14.3 million for the 12 months ending January 2016.

Press release (pdf)

Important notice for users

You are about to access Hikma historic archive material. Any reference in these archives to Hikma products or their uses may not reflect current medical knowledge and should not be used as a source of information on the present product label, efficacy data, or safety data. Please refer to your approved national product label (SmPC) for current product information.

I have read this warning and will not be using any of the contained product information for clinical purposes.