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Mar 03

Actavis receives final FDA authorization for Zolpidem ER Tablets Actavis.

Actavis receives final FDA authorization for Zolpidem ER Tablets Actavis, an international generic pharmaceuticals organization, today announced that it has received final approval from the united states Food & Medication Administration to advertise Zolpidem Tartrate Extended-Discharge Tablets USP, 12.5 mg CIV.5 mg enables Actavis to provide both strengths to meet up the needs of our customers.’.But perhaps, the two most bothersome of all Accutane side effects are its potential to cause severe birth defects if used by women that are pregnant or ladies that became pregnant while taking the medication and the suggested web page link between your intake of Accutane and the adjustments in mood, severe depressive disorder and suicidal thoughts. Since, Isotretinoin could be harmful to the fetus, it should not be utilized during pregnancy and women should avoid pregnancy for at least a month after the usage of Accutane.