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11. Importation of certain FDA approved human prescription drugs, including biological products, and combination products under section 801(d)(1)(b) of the Federal Food, Drug, and Cosmetic Act

18. Oncology therapeutic radiopharmaceuticals: nonclinical studies and labeling recommendations

19. Wholesale distributor verification requirement for saleable returned drug product: compliance policy

20. Human prescription drug and biological products: labeling for dosing based on weight or body surface area for ready-to-use containers : “dose banding” : guidance for industry