This is a legal form that was released by the U.S. Department of Health and Human Services - U.S. Food and Drug Administration on June 1, 2021 and used country-wide. As of today, no separate filing guidelines for the form are provided by the issuing department.
Q: What is Form FDA2301?
A: Form FDA2301 is a document used to transmit periodic reports and promotional material for new animal drugs.
Q: What is the purpose of Form FDA2301?
A: The purpose of Form FDA2301 is to provide a means for the submission of periodic reports and promotional material for new animal drugs.
Q: Who is required to submit Form FDA2301?
A: Manufacturers of new animal drugs are required to submit Form FDA2301.
Q: What information is included in Form FDA2301?
A: Form FDA2301 includes information about the new animal drug, the manufacturer, and details of the periodic reports or promotional material being submitted.
Q: How is Form FDA2301 submitted?
A: Form FDA2301 can be submitted electronically or in paper form.
Q: Are there any fees associated with submitting Form FDA2301?
A: There are no fees associated with submitting Form FDA2301.
Form Details:
Download a fillable version of Form FDA2301 by clicking the link below or browse more documents and templates provided by the U.S. Department of Health and Human Services - U.S. Food and Drug Administration.