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Code of Federal Regulations Title 21. Food and Drugs § 21.330.11 NDA deviations from applicable monograph

Current as of January 02, 2025 | Updated by Findlaw Staff

A new drug application requesting approval of an OTC drug deviating in any respect from a monograph that has become final shall be in the form required by § 314.50 of this chapter, but shall include a statement that the product meets all conditions of the applicable monograph except for the deviation for which approval is requested and may omit all information except that pertinent to the deviation.

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Cite this article: FindLaw.com - Code of Federal Regulations Title 21. Food and Drugs § 21.330.11 NDA deviations from applicable monograph - last updated January 02, 2025 | https://codes.findlaw.com/cfr/title-21-food-and-drugs/cfr-sect-21-330-11/

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