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Guidance on Residual Solvent in Animal Drugs

04/03/2015

Federal Register Notice: FDA is making available a guidance for industry entitled Residual Solvents in Animal Drug Products; Questions and Answers. The questions and answers guidance addresses the USP General Chapter 467 Residual Solvents that applies to both human and veterinary drugs and to compendial and non-compendial drug products. This document answers questions on the Center for Veterinary Medicine’s implementation of USP 467 Residual Solvents. To download this guidance, click here. To view this notice, click here.

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