CFR Title 21 Parts 1300 to End Food and Drugs Revised as of April 1, 2018

CFR Title 21 Parts 1300 to End|Code of Federal Regulations Title 21 Food and Drugs, 2018 Edition

Title 21—FOOD AND DRUGS is composed of nine volumes. The parts in these volumes are arranged in the following order: Parts 1–99, 100–169, 170–199, 200–299, 300–499, 500–599, 600–799, 800–1299 and 1300 to end. The first eight volumes, containing parts 1–1299, comprise Chapter I—Food and Drug Administration, Department of Health and Human Services. The ninth volume, containing part 1300 to end, includes Chapter II—Drug Enforcement Administration, Department of Justice, and Chapter III—Office of National Drug Control Policy. The contents of these volumes represent all current regulations codified under this title of the CFR as of April 1, 2018.

Title 21–Food and Drugs
(This book contains part 1300 to End)
Part
CHAPTER II—Drug Enforcement Administration, Department of Justice .................................................................. 1301
CHAPTER III—Office of National Drug Control Policy ............ 1401

Table of Contents
Page
Explanation ................................................................................................ v
Title 21:
Chapter II—Drug Enforcement Administration, Department of Justice ........................................................................... 3
Chapter III—Office of National Drug Control Policy ...................... 277
Finding Aids:
Table of CFR Titles and Chapters ....................................................... 287
Alphabetical List of Agencies Appearing in the CFR ......................... 307
List of CFR Sections Affected ............................................................. 317

CHAPTER II—DRUG ENFORCEMENT ADMINISTRATION, DEPARTMENT OF JUSTICE
Part Page
1300 Definitions .............................................................. 5
1301 Registration of manufacturers, distributors, and dispensers of controlled substances ..................... 23
1302 Labeling and packaging requirements for controlled substances ................................................ 58
1303 Quotas ..................................................................... 60
1304 Records and reports of registrants .......................... 68
1305 Orders for schedule I and II controlled substances 88
1306 Prescriptions ........................................................... 96
1307 Miscellaneous .......................................................... 108
1308 Schedules of controlled substances ......................... 110
1309 Registration of manufacturers, distributors, importers and exporters of list I chemicals .............. 137
1310 Records and reports of listed chemicals and certain machines; importation and exportation of certain machines ....................................................... 148
1311 Requirements for electronic orders and prescriptions..................................................................... 175
1312 Importation and exportation of controlled substances................................................................ 199
1313 Importation and exportation of list I and list II chemicals ............................................................. 219
1314 Retail sale of scheduled listed chemical products ... 232
1315 Importation and production quotas for ephedrine, pseudoephedrine, and phenylpropanolamine ........ 240
1316 Administrative functions, practices, and procedures..................................................................... 251
1317 Disposal ................................................................... 262
1321 DEA Mailing addresses ............................................ 272
1322–1399 [Reserved]

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