Code Of Federal Regulations Title 21 Volume 1 April 1 2015
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Code Of Federal Regulations Title 21 Volume 1 April 1 2015
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Author : Office of the Federal Register
language : en
Publisher: Regulations Press
Release Date : 2016-02-24
Code Of Federal Regulations Title 21 Volume 1 April 1 2015 written by Office of the Federal Register and has been published by Regulations Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-02-24 with categories.
21 CFR Parts 0-99 covers a range of topics including general administrative rulings and decisions; to protection of privacy, environmental impact considerations, pharmaceutical manufacturing practices and reports for devices within the United States and European community; color additives in food, drugs, and cosmetics, and more. This volume would be appropriate for the general public, plus pharmacy and start up health care manufacturers, as well as food, drug, and cosmetic company personnel interested in developing products to be disseminated within the United States of America. Code of Federal Regulations Title 21, Volume 1, April 1, 2015 Containing parts Parts 1 to 99 Part 1; GENERAL ENFORCEMENT REGULATIONS Part 2; GENERAL ADMINISTRATIVE RULINGS AND DECISIONS Part 3; PRODUCT JURISDICTION Part 4; REGULATION OF COMBINATION PRODUCTS Part 5; ORGANIZATION Part 7; ENFORCEMENT POLICY Part 10; ADMINISTRATIVE PRACTICES AND PROCEDURES Part 11; ELECTRONIC RECORDS; ELECTRONIC SIGNATURES Part 12; FORMAL EVIDENTIARY PUBLIC HEARING Part 13; PUBLIC HEARING BEFORE A PUBLIC BOARD OF INQUIRY Part 14; PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE Part 15; PUBLIC HEARING BEFORE THE COMMISSIONER Part 16; REGULATORY HEARING BEFORE THE FOOD AND DRUG ADMINISTRATION Part 17; CIVIL MONEY PENALTIES HEARINGS Part 19; STANDARDS OF CONDUCT AND CONFLICTS OF INTEREST Part 20; PUBLIC INFORMATION Part 21; PROTECTION OF PRIVACY Part 25; ENVIRONMENTAL IMPACT CONSIDERATIONS Part 26; MUTUAL RECOGNITION OF PHARMACEUTICAL GOOD MANUFACTURING PRACTICE REPORTS, MEDICAL DEVICE QUALITY SYSTEM AUDIT REPORTS, AND CERTAIN MEDICAL DEVICE PRODUCT EVALUATION REPORTS: UNITED STATES AND THE EUROPEAN COMMUNITY Part 50; PROTECTION OF HUMAN SUBJECTS Part 54; FINANCIAL DISCLOSURE BY CLINICAL INVESTIGATORS Part 56; INSTITUTIONAL REVIEW BOARDS Part 58; GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES Part 60; PATENT TERM RESTORATION Part 70; COLOR ADDITIVES Part 71; COLOR ADDITIVE PETITIONS Part 73; LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Part 74; LISTING OF COLOR ADDITIVES SUBJECT TO CERTIFICATION Part 80; COLOR ADDITIVE CERTIFICATION Part 81; GENERAL SPECIFICATIONS AND GENERAL RESTRICTIONS FOR PROVISIONAL COLOR ADDITIVES FOR USE IN FOODS, DRUGS, AND COSMETICS Part 82; LISTING OF CERTIFIED PROVISIONALLY LISTED COLORS AND SPECIFICATIONS Parts 83-98; Reserved Part 99; DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES
Code Of Federal Regulations Title 21 Volume 7 April 1 2015
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Author : Office of the Federal Register
language : en
Publisher: Regulations Press
Release Date : 2016-02-24
Code Of Federal Regulations Title 21 Volume 7 April 1 2015 written by Office of the Federal Register and has been published by Regulations Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-02-24 with categories.
21 CFR Parts 600 - 799 covers biological products, licensing, standards, and cosmetics. Code of Federal Regulations Title 21, Volume 7, April 1, 2015 Containing parts Parts 600 to 799 Part 600; BIOLOGICAL PRODUCTS: GENERAL Part 601; LICENSING Part 606; CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS Part 607; ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS Part 610; GENERAL BIOLOGICAL PRODUCTS STANDARDS Part 630; GENERAL REQUIREMENTS FOR BLOOD, BLOOD COMPONENTS, AND BLOOD DERIVATIVES Part 640; ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS Part 660; ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS Part 680; ADDITIONAL STANDARDS FOR MISCELLANEOUS PRODUCTS Part 700; GENERAL Part 701; COSMETIC LABELING Part 710; VOLUNTARY REGISTRATION OF COSMETIC PRODUCT ESTABLISHMENTS Part 720; VOLUNTARY FILING OF COSMETIC PRODUCT INGREDIENT COMPOSITION STATEMENTS Part 740; COSMETIC PRODUCT WARNING STATEMENTS Parts 741-799; Reserved
Code Of Federal Regulations Title 21 Volume 3 April 1 2015
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Author : Office of the Federal Register
language : en
Publisher: Regulations Press
Release Date : 2016-02-24
Code Of Federal Regulations Title 21 Volume 3 April 1 2015 written by Office of the Federal Register and has been published by Regulations Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-02-24 with categories.
21 CFR Part 170 to 199 contains food additives, production, processing, and handling of food, indirect food additives, such as paper, cardboard, and hand sanitizers, dietary supplements, and more. Code of Federal Regulations Title 21, Volume 3, April 1, 2015 Containing parts Parts 170 to 199 Part 170; FOOD ADDITIVES Part 171; FOOD ADDITIVE PETITIONS Part 172; FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION Part 173; SECONDARY DIRECT FOOD ADDITIVES PERMITTED IN FOOD FOR HUMAN CONSUMPTION Part 174; INDIRECT FOOD ADDITIVES: GENERAL Part 175; INDIRECT FOOD ADDITIVES: ADHESIVES AND COMPONENTS OF COATINGS Part 176; INDIRECT FOOD ADDITIVES: PAPER AND PAPERBOARD COMPONENTS Part 177; INDIRECT FOOD ADDITIVES: POLYMERS Part 178; INDIRECT FOOD ADDITIVES: ADJUVANTS, PRODUCTION AIDS, AND SANITIZERS Part 179; IRRADIATION IN THE PRODUCTION, PROCESSING AND HANDLING OF FOOD Part 180; FOOD ADDITIVES PERMITTED IN FOOD OR IN CONTACT WITH FOOD ON AN INTERIM BASIS PENDING ADDITIONAL STUDY Part 181; PRIOR-SANCTIONED FOOD INGREDIENTS Part 182; SUBSTANCES GENERALLY RECOGNIZED AS SAFE Part 184; DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Part 186; INDIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Part 189; SUBSTANCES PROHIBITED FROM USE IN HUMAN FOOD Part 190; DIETARY SUPPLEMENTS Parts 191-199; Reserved
Code Of Federal Regulations Title 21 Volume 4 April 1 2015
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Author : Office of the Federal Register
language : en
Publisher: Regulations Press
Release Date : 2016-02-24
Code Of Federal Regulations Title 21 Volume 4 April 1 2015 written by Office of the Federal Register and has been published by Regulations Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-02-24 with categories.
21 CFR Parts 200-299 covers prescription drug products for human use, manufacturing, labeling, processing, and packing practices, official drug names, and more. Code of Federal Regulations Title 21, Volume 4, April 1, 2015 Containing parts Parts 200 to 299 Part 200; GENERAL Part 201; LABELING Part 202; PRESCRIPTION DRUG ADVERTISING Part 203; PRESCRIPTION DRUG MARKETING Part 205; GUIDELINES FOR STATE LICENSING OF WHOLESALE PRESCRIPTION DRUG DISTRIBUTORS Part 206; IMPRINTING OF SOLID ORAL DOSAGE FORM DRUG PRODUCTS FOR HUMAN USE Part 207; REGISTRATION OF PRODUCERS OF DRUGS AND LISTING OF DRUGS IN COMMERCIAL DISTRIBUTION Part 208; MEDICATION GUIDES FOR PRESCRIPTION DRUG PRODUCTS Part 209; REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFFECTS STATEMENT Part 210; CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL Part 211; CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS Part 212; CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS Part 216; PHARMACY COMPOUNDING Part 225; CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS Part 226; CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES Part 250; SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS Part 290; CONTROLLED DRUGS Part 299; DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES
Code Of Federal Regulations Title 21 Volume 9 April 1 2015
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Author : Office of the Federal Register
language : en
Publisher: Regulations Press
Release Date : 2016-02-24
Code Of Federal Regulations Title 21 Volume 9 April 1 2015 written by Office of the Federal Register and has been published by Regulations Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-02-24 with Law categories.
21 CFR Parts 1300-End covers drug enforcement including the labeling and packaging requirements for controlled substances, prescriptions, requirements for electronic orders for prescriptions, importation and exportation of listing of chemicals, and more. Code of Federal Regulations Title 21, Volume 9, April 1, 2015 Containing parts Part 1300 to End Part 1300; DEFINITIONS Part 1301; REGISTRATION OF MANUFACTURERS, DISTRIBUTORS, AND DISPENSERS OF CONTROLLED SUBSTANCES Part 1302; LABELING AND PACKAGING REQUIREMENTS FOR CONTROLLED SUBSTANCES Part 1303; QUOTAS Part 1304; RECORDS AND REPORTS OF REGISTRANTS Part 1305; ORDERS FOR SCHEDULE I AND II CONTROLLED SUBSTANCES Part 1306; PRESCRIPTIONS Part 1307; MISCELLANEOUS Part 1308; SCHEDULES OF CONTROLLED SUBSTANCES Part 1309; REGISTRATION OF MANUFACTURERS, DISTRIBUTORS, IMPORTERS AND EXPORTERS OF LIST I CHEMICALS Part 1310; RECORDS AND REPORTS OF LISTED CHEMICALS AND CERTAIN MACHINES Part 1311; REQUIREMENTS FOR ELECTRONIC ORDERS AND PRESCRIPTIONS Part 1312; IMPORTATION AND EXPORTATION OF CONTROLLED SUBSTANCES Part 1313; IMPORTATION AND EXPORTATION OF LIST I AND LIST II CHEMICALS Part 1314; RETAIL SALE OF SCHEDULED LISTED CHEMICAL PRODUCTS Part 1315; IMPORTATION AND PRODUCTION QUOTAS FOR EPHEDRINE, PSEUDOEPHEDRINE, AND PHENYLPROPANOLAMINE Part 1316; ADMINISTRATIVE FUNCTIONS, PRACTICES, AND PROCEDURES Part 1317; DISPOSAL Part 1321; DEA MAILING ADDRESSES Parts 1322-1399; Reserved Part 1400; Reserved Part 1401; PUBLIC AVAILABILITY OF INFORMATION Part 1402; MANDATORY DECLASSIFICATION REVIEW Parts 1403-1499; Reserved
Code Of Federal Regulations Title 21 Food And Drugs Pt 800 1299 Revised As Of April 1 2015
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Author : Food and Drug Administration (U S )
language : en
Publisher: Office of the Federal Register
Release Date : 2015-04-01
Code Of Federal Regulations Title 21 Food And Drugs Pt 800 1299 Revised As Of April 1 2015 written by Food and Drug Administration (U S ) and has been published by Office of the Federal Register this book supported file pdf, txt, epub, kindle and other format this book has been release on 2015-04-01 with Business & Economics categories.
This print ISBN is the U.S. Federal Government Official edition of this title. 21 CFR Parts 800 to 1299 covers the U. S. Food and Drug Administration within the U.S. Department of Health and Human Services. Within this volume, you will find rules, procedures, and regulations pertaining to medical devices, such as cardiovascular devices, dentistry devices, orthopedic, gastroenterology-urology, in vitro, anestheology, and more. Plus, you will find rules, procedures, and regulations relating to mammography quality standards, radiological health, tobacco products, human tissue intended for transplantation, and more. Keywords: health care; healthcare; healthcare policy; medical devices; healthcare personnel; hospital personnel; physicians; out-patient clinical staff; medical technicians; cigarette tobacco and advertising, smoking; tobacco; food and drug administration; fda; FDA; united states food and drug administration; united states department of health and human services; HHS; hhs; medical technology; 21 CFR Parts 800-1299; cfr 21 parts 800-1299; cfr 21 Parts 800-1299; 21 CFR; 21 cfr; 21 code of federal regulations;
Code Of Federal Regulations Title 21 Volume 8 April 1 2015
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Author : Office of the Federal Register
language : en
Publisher: Regulations Press
Release Date : 2016-02-24
Code Of Federal Regulations Title 21 Volume 8 April 1 2015 written by Office of the Federal Register and has been published by Regulations Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-02-24 with categories.
21 CFR Parts 800 to 1299 covers the U. S. Food and Drug Administration within the U.S. Department of Health and Human Services. Within this volume, you will find rules, procedures, and regulations pertaining to medical devices, such as cardiovascular devices, dentistry devices, orthopedic, gastroenterology-urology, in vitro, anesthesiology, and more. Plus, you will find rules, procedures, and regulations relating to mammography quality standards, radiological health, tobacco products, human tissue intended for transplantation, and more. Health care device manufacturers, hospital radiological and other medical technicians and departments, physicians, nurses, out-patient clinics' personnel, and health care policy advocates may be interested in this volume. Code of Federal Regulations Title 21, Volume 8, April 1, 2015 Containing parts Parts 800 to 1299 Part 800; GENERAL Part 801; LABELING Part 803; MEDICAL DEVICE REPORTING; (Eff. Until 8-14-15) Part 806; MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS Part 807; ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES Part 808; EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS Part 809; IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE Part 810; MEDICAL DEVICE RECALL AUTHORITY Part 812; INVESTIGATIONAL DEVICE EXEMPTIONS Part 813; Reserved Part 814; PREMARKET APPROVAL OF MEDICAL DEVICES Part 820; QUALITY SYSTEM REGULATION Part 821; MEDICAL DEVICE TRACKING REQUIREMENTS Part 822; POSTMARKET SURVEILLANCE Part 830; UNIQUE DEVICE IDENTIFICATION Part 860; MEDICAL DEVICE CLASSIFICATION PROCEDURES Part 861; PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT Part 862; CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES Part 864; HEMATOLOGY AND PATHOLOGY DEVICES Part 866; IMMUNOLOGY AND MICROBIOLOGY DEVICES Part 868; ANESTHESIOLOGY DEVICES Part 870; CARDIOVASCULAR DEVICES Part 872; DENTAL DEVICES Part 874; EAR, NOSE, AND THROAT DEVICES Part 876; GASTROENTEROLOGY-UROLOGY DEVICES Part 878; GENERAL AND PLASTIC SURGERY DEVICES Part 880; GENERAL HOSPITAL AND PERSONAL USE DEVICES Part 882; NEUROLOGICAL DEVICES Part 884; OBSTETRICAL AND GYNECOLOGICAL DEVICES Part 886; OPHTHALMIC DEVICES Part 888; ORTHOPEDIC DEVICES Part 890; PHYSICAL MEDICINE DEVICES Part 892; RADIOLOGY DEVICES Part 895; BANNED DEVICES Part 898; PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES Part 900; MAMMOGRAPHY Part 1000; GENERAL Part 1002; RECORDS AND REPORTS Part 1003; NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY Part 1004; REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS Part 1005; IMPORTATION OF ELECTRONIC PRODUCTS Part 1010; PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL Part 1020; PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS Part 1030; PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS Part 1040; PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS Part 1050; PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS Part 1107; ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS Part 1140; CIGARETTES AND SMOKELESS TOBACCO Part 1141; CIGARETTE PACKAGE AND ADVERTISING WARNINGS Part 1150; USER FEES Part 1210; REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT Part 1230; REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT Part 1240; CONTROL OF COMMUNICABLE DISEASES Part 1250; INTERSTATE CONVEYANCE SANITATION Parts 1251-1269; Reserved Part 1270; HUMAN TISSUE INTENDED FOR TRANSPLANTATION Part 1271; HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS Parts 1272-1299; Reserved
Code Of Federal Regulations Title 21 Food And Drugs Pt 1 99 Revised As Of April 1 2015
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Author : Office of the Federal Register (U S )
language : en
Publisher: Office of the Federal Register
Release Date : 2015-06-18
Code Of Federal Regulations Title 21 Food And Drugs Pt 1 99 Revised As Of April 1 2015 written by Office of the Federal Register (U S ) and has been published by Office of the Federal Register this book supported file pdf, txt, epub, kindle and other format this book has been release on 2015-06-18 with Law categories.
The Code of Federal Regulations is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the United States Federal Government. This official edition of the 21 CFR Parts 0-99 covers a range of topics including general adminsitrative rulings and decisions ....to protection of privacy, environmental impact considerations, pharmaceutical manufacturing practices and reports for devices within the United States and European community; color additives in food, drugs, and cosmetics, and more. This volume would be appropriate for the general public, plus pharma and start up healthcare manufacturers, as well as food, drug, and cosmetic company personnel interested in developing products to be diseeminated within the United States of America.
Code Of Federal Regulations Title 21 Volume 6 April 1 2015
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Author : Office of the Federal Register
language : en
Publisher: Regulations Press
Release Date : 2016-02-24
Code Of Federal Regulations Title 21 Volume 6 April 1 2015 written by Office of the Federal Register and has been published by Regulations Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-02-24 with categories.
21 CFR Parts 500-599 covers animal drug products, dosages, animal food labeling, animal drug applications, and more. Code of Federal Regulations Title 21, Volume 6, April 1, 2015 Containing parts Parts 500 to 599 Part 500; GENERAL Part 501; ANIMAL FOOD LABELING Part 502; COMMON OR USUAL NAMES FOR NONSTANDARDIZED ANIMAL FOODS Part 509; UNAVOIDABLE CONTAMINANTS IN ANIMAL FOOD AND FOOD-PACKAGING MATERIAL Part 510; NEW ANIMAL DRUGS Part 511; NEW ANIMAL DRUGS FOR INVESTIGATIONAL USE Part 514; NEW ANIMAL DRUG APPLICATIONS Part 515; MEDICATED FEED MILL LICENSE Part 516; NEW ANIMAL DRUGS FOR MINOR USE AND MINOR SPECIES Part 520; ORAL DOSAGE FORM NEW ANIMAL DRUGS Part 522; IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL DRUGS Part 524; OPHTHALMIC AND TOPICAL DOSAGE FORM NEW ANIMAL DRUGS Part 526; INTRAMAMMARY DOSAGE FORM NEW ANIMAL DRUGS Part 528; NEW ANIMAL DRUGS IN GENETICALLY ENGINEERED ANIMALS Part 529; CERTAIN OTHER DOSAGE FORM NEW ANIMAL DRUGS Part 530; EXTRALABEL DRUG USE IN ANIMALS Part 556; TOLERANCES FOR RESIDUES OF NEW ANIMAL DRUGS IN FOOD Part 558; NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS Part 564; Reserved Part 570; FOOD ADDITIVES Part 571; FOOD ADDITIVE PETITIONS Part 573; FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Part 579; IRRADIATION IN THE PRODUCTION, PROCESSING, AND HANDLING OF ANIMAL FEED AND PET FOOD Part 582; SUBSTANCES GENERALLY RECOGNIZED AS SAFE Part 584; FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE IN FEED AND DRINKING WATER OF ANIMALS Part 589; SUBSTANCES PROHIBITED FROM USE IN ANIMAL FOOD OR FEED Parts 590-599; Reserved
Code Of Federal Regulations Title 21 Volume 5 April 1 2015
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Author : Office of the Federal Register
language : en
Publisher: Regulations Press
Release Date : 2016-02-24
Code Of Federal Regulations Title 21 Volume 5 April 1 2015 written by Office of the Federal Register and has been published by Regulations Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-02-24 with categories.
Code of Federal Regulations Title 21, Volume 5, April 1, 2015 Containing parts Parts 300 to 499 Part 300; GENERAL Part 310; NEW DRUGS Part 312; INVESTIGATIONAL NEW DRUG APPLICATION Part 314; APPLICATIONS FOR FDA APPROVAL TO MARKET A NEW DRUG Part 315; DIAGNOSTIC RADIOPHARMACEUTICALS Part 316; ORPHAN DRUGS Part 317; QUALIFYING PATHOGENS Part 320; BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS Part 328; OVER-THE-COUNTER DRUG PRODUCTS INTENDED FOR ORAL INGESTION THAT CONTAIN ALCOHOL Part 329; NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT Part 330; OVER-THE-COUNTER (OTC) HUMAN DRUGS WHICH ARE GENERALLY RECOGNIZED AS SAFE AND EFFECTIVE AND NOT MISBRANDED Part 331; ANTACID PRODUCTS FOR OVER-THE-COUNTER (OTC) HUMAN USE Part 332; ANTIFLATULENT PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 333; TOPICAL ANTIMICROBIAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 335; ANTIDIARRHEAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 336; ANTIEMETIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 338; NIGHTTIME SLEEP-AID DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 340; STIMULANT DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 341; COLD, COUGH, ALLERGY, BRONCHODILATOR, AND ANTIASTHMATIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 343; INTERNAL ANALGESIC, ANTIPYRETIC, AND ANTIRHEUMATIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 344; TOPICAL OTIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 346; ANORECTAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 347; SKIN PROTECTANT DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 348; EXTERNAL ANALGESIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 349; OPHTHALMIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 350; ANTIPERSPIRANT DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 352; SUNSCREEN DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [STAYED INDEFINITELY] Part 355; ANTICARIES DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 357; MISCELLANEOUS INTERNAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 358; MISCELLANEOUS EXTERNAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Part 361; PRESCRIPTION DRUGS FOR HUMAN USE GENERALLY RECOGNIZED AS SAFE AND EFFECTIVE AND NOT MISBRANDED: DRUGS USED IN RESEARCH Part 369; INTERPRETATIVE STATEMENTS RE WARNINGS ON DRUGS AND DEVICES FOR OVER-THE-COUNTER SALE Parts 370-499; Reserved