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Zdrowie i gospodarka · 07/08/1998

FDA Clears Acyclovir 200-Mg Tablets for Approval, Citing Lack of Safety or Effectiveness Concerns

The US Food and Drug Administration (FDA) has made a determination that acyclovir 200-milligram tablets were not withdrawn from sale due to safety or effectiveness concerns, paving the way for the approval of abbreviated new drug applications (ANDA's) for these tablets.

Source: Federal Register — Food and Drug AdministrationOpen original release →