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[A1]

Electronic Code of Federal Regulations

e-CFR data is current as of July 1, 2020

Title 21 → Chapter I → Subchapter E → Part 530

TITLE 21—Food and Drugs

CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

SUBCHAPTER E—ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS

PART 530—EXTRALABEL DRUG USE IN ANIMALS

rule

Subpart A—GENERAL PROVISIONS

§530.1
Scope.
§530.2
Purpose.
§530.3
Definitions.
§530.4
Advertising and promotion.
§530.5
Veterinary records.
rule

Subpart B—RULES AND PROVISIONS FOR EXTRALABEL USES OF DRUGS IN ANIMALS

§530.10
Provision permitting extralabel use of animal drugs.
§530.11
Limitations.
§530.12
Labeling.
§530.13
Extralabel use from compounding of approved new animal and approved human drugs.
rule

Subpart C—SPECIFIC PROVISIONS RELATING TO EXTRALABEL USE OF ANIMAL AND HUMAN DRUGS IN FOOD-PRODUCING ANIMALS

§530.20
Conditions for permitted extralabel animal and human drug use in food-producing animals.
§530.21
Prohibitions for food-producing animals.
§530.22
Safe levels and analytical methods for food-producing animals.
§530.23
Procedure for setting and announcing safe levels.
§530.24
Procedure for announcing analytical methods for drug residue quantification.
§530.25
Orders prohibiting extralabel uses for drugs in food-producing animals.
rule

Subpart D—EXTRALABEL USE OF HUMAN AND ANIMAL DRUGS IN ANIMALS NOT INTENDED FOR HUMAN CONSUMPTION

§530.30
Extralabel drug use in nonfood animals.
rule

Subpart E—SAFE LEVELS FOR EXTRALABEL USE OF DRUGS IN ANIMALS AND DRUGS PROHIBITED FROM EXTRALABEL USE IN ANIMALS

§530.40
Safe levels and availability of analytical methods.
§530.41
Drugs prohibited for extralabel use in animals.

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