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Registration Requirements for Importers and Manufacturers of Prescription Drug Products Containing Ephedrine, Pseudoephedrine, or Phenylpropanolamine (US Drug Enforcement Administration Regulation) (DEA) (2018 Edition) The Law Library

Registration Requirements for Importers and Manufacturers of Prescription Drug Products Containing Ephedrine, Pseudoephedrine, or Phenylpropanolamine (US Drug Enforcement Administration Regulation) (DEA) (2018 Edition) The Law Library presents the complete text of the Registration Requirements for Importers and Manufacturers of Prescription Drug Products Containing Ephedrine, Pseudoephedrine, or Phenylpropanolamine (US Drug Enforcement Administration Regulation) (DEA) (2018 Edition). Updated as of May 29, 2018 The Drug Enforcement Administration (DEA) is amending its registration regulations to ensure that a registration is obtained for every location where ephedrine, pseudoephedrine, or phenylpropanolamine, or drug products containing one of these chemicals, are imported or manufactured. These amendments will make it possible to establish the system of quotas and assessment of annual needs for the importation and manufacture of these chemicals that Congress mandated in the Combat Methamphetamine Epidemic Act of 2005. This book contains: - The complete text of the Registration Requirements for Importers and Manufacturers of Prescription Drug Products Containing Ephedrine, Pseudoephedrine, or Phenylpropanolamine (US Drug Enforcement Administration Regulation) (DEA) (2018 Edition) - A table of contents with the page number of each section