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3. Quality attribute considerations for chewable tablets

11. Ambulatory surgery facilities: a comprehensive review of medication error reports in Pennsylvania

12. Temporary policy on repackaging or combining propofol drug products during the COVID-19 public health emergency

14. 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

21. Oncology therapeutic radiopharmaceuticals: nonclinical studies and labeling recommendations

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

23. 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