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Negocios · 15/11/19961 min de lectura
Determination That Ibuprofen 200-Milligram Capsule Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness
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Resumen
The Food and Drug Administration (FDA) has determined that ibuprofen (Midol ) 200-milligram (mg) capsule was not withdrawn from sale for reasons of safety or effectiveness. This determination will allow FDA to approve abbreviated new drug applications (ANDA's) for ibuprofen 200-mg capsule.
Idioma original de la fuente: Federal Register — Food and Drug AdministrationAbrir el comunicado original →