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title 21
Food and Drugs
chapter I-i3
CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)
part 207
PART 207—REQUIREMENTS FOR FOREIGN AND DOMESTIC ESTABLISHMENT REGISTRATION AND LISTING FOR HUMAN DRUGS, INCLUDING DRUGS THAT ARE REGULATED UNDER A BIOLOGICS LICENSE APPLICATION, AND ANIMAL DRUGS, AND THE NATIONAL DRUG CODE
subpart C
Subpart C—National Drug Code
Subpart C. Subpart C—National Drug Code
§ 207.33 - What is the National Drug Code (NDC), how is it assigned, and what are its requirements?
§ 207.35 - What changes require a new NDC?
§ 207.37 - What restrictions pertain to the use of the NDC?
