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[A1]

 

Electronic Code of Federal Regulations

e-CFR data is current as of November 18, 2019

Title 21 → Chapter I → Subchapter E → Part 500

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 500—GENERAL

rule

Subpart A—[RESERVED]

rule

Subpart B—SPECIFIC ADMINISTRATIVE RULINGS AND DECISIONS

§500.23
Thermally processed low-acid foods packaged in hermetically sealed containers.
§500.24
Emergency permit control.
§500.25
Anthelmintic drugs for use in animals.
§500.26
Timed-release dosage form drugs.
§500.27
Methylene blue-containing drugs for use in animals.
§500.29
Gentian violet for use in animal feed.
§500.30
Gentian violet for animal drug use.
§500.45
Use of polychlorinated biphenyls (PCB's) in the production, handling, and storage of animal feed.
§500.46
Hexachlorophene in animal drugs.
§500.50
Propylene glycol in or on cat food.
rule

Subpart C—ANIMAL DRUG LABELING REQUIREMENTS

§500.51
Labeling of animal drugs; misbranding.
§500.52
Use of terms such as “tonic”, “tone”, “toner”, or “conditioner” in the labeling of preparations intended for use in or on animals.
§500.55
Exemption from certain drug-labeling requirements.
rule

Subpart D—REQUIREMENTS FOR SPECIFIC ANIMAL DRUGS

§500.65
Epinephrine injection 1:1,000 in 10-milliliter containers for emergency treatment of anaphylactoid shock in cattle, horses, sheep, and swine.
rule

Subpart E—REGULATION OF CARCINOGENIC COMPOUNDS USED IN FOOD-PRODUCING ANIMALS

§500.80
Scope of this subpart.
§500.82
Definitions.
§500.84
Conditions for approval of the sponsored compound.
§500.86
Marker residue and target tissue.
§500.88
Regulatory method.
§500.90
Waiver of requirements.
§500.92
Implementation.
rule

Subpart F—METHODS FOR DETECTION OF RESIDUES OF CARCINOGENIC COMPOUNDS USED IN FOOD-PRODUCING ANIMALS

§500.1410
N-methyl-2-pyrrolidone.

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