"The U.S. Food and Drug Administration today notified Ranbaxy Laboratories, Ltd., that it is prohibited from manufacturing and distributing active pharmaceutical ingredients (APIs) from its facility in Toansa, India, for FDA-regulated drug product"...
HYPERSENSITIVITY TO ANY COMPONENT OF THE VACCINE, INCLUDING THIMEROSAL AND DIPHTHERIA TOXOID, IS A CONTRAINDICATION TO USE OF THIS VACCINE.
Last reviewed on RxList: 3/9/2009
This monograph has been modified to include the generic and brand name in many instances.
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