"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"...
In the event of a fluid or solute overload during parenteral therapy, reevaluate the patient's condition and institute appropriate corrective treatment.
Severe liver disease and hepatic coma.
Metabolic disorders associated with impaired nitrogen utilization.
Hypersensitivity to one or more amino acids.
Last reviewed on RxList: 12/18/2008
This monograph has been modified to include the generic and brand name in many instances.
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