Health and Human Services Department, Food and Drug Administration
The Food and Drug Administration (FDA) is announcing that Zeneca Pharmaceuticals Inc., has filed an application requesting conditional approval for the export of the human drug Arimidex (Anastrozole) 1 mg tablet to the United Kingdom.
Other Federal Register documents from the same docket.
Mutual Recognition of the Food and Drug Administration and European Community Member State Conformity Assessment Procedures; Pharmaceutical GMP Inspection Reports, Medical Device Quality System Evaluation Reports, and Certain Medical Device Premarket Evaluation Reports
Drug Export; Arimidex (Anastrozole) 1 Milligram (mg) Tablet
Citation: 60 FR 33810
