CFR 21(PTS500-599) : 0

Superseded

Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View superseded by

FOOD AND DRUGS - FOOD AND DRUG ADMINISTRATION, CHAPTER 1 DEPARTMENT OF HEALTH AND HUMAN SERVICES - PARTS 500-599

Available format(s):

Superseded date: 20-11-2019

Language(s):

Published date:

Publisher: Code of Federal Regulations

Table of Contents - (Show below) - (Hide below)

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 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 forms
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
Part 590-599 - [Reserved]

General Product Information - (Show below) - (Hide below)

Document Type	Standard
ISBN
Pages
Published
Publisher	Code of Federal Regulations
Status	Superseded
Superseded By	CFR 21 PART 500-599:2019

Standards Referenced By This Book - (Show below) - (Hide below)

ANSI/AAMI/IEC 60601-1-2:2014	MEDICAL ELECTRICAL EQUIPMENT - PART 1-2: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: ELECTROMAGNETIC DISTURBANCES - REQUIREMENTS AND TESTS
DD ISO/TS 22224:2009	Health informatics. Electronic reporting of adverse drug reactions
DI-TCSP-82040 Base Document:2016	RESEARCH AND DEVELOPMENT OF MEDICAL PRODUCTS REGULATED BY THE U.S. FOOD AND DRUG ADMINISTRATION (FDA)
ISO/TS 22224:2009	Health informatics Electronic reporting of adverse drug reactions
IEC 60601-1-2:2007	Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic compatibility - Requirements and tests

Categories associated with this Standard - (Show below) - (Hide below)

Sub-Categories associated with this Standard - (Show below) - (Hide below)

Sorry this product is not available in your region.

Add To Cart