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20 results 379j-13
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Exact match Title 21 Title 21 / Chapter 9 FEDERAL FOOD, DRUG, AND COSMETIC ACT / Subchapter VII GENERAL AUTHORITY / Part C Fees / Subpart 4 fees relating to animal drugs / Section 379j–13

21 U.S.C. § 379j–13

Reauthorization; reporting requirements

Part C Fees / Subpart 4 fees relating to animal drugs

Exact citation match for 21 USC § 379J-13

Title 21 Title 21 / Section 379j–11

21 U.S.C. § 379j–11

Definitions

Part C Fees / Subpart 4 fees relating to animal drugs

Definitions

Title 21 Title 21 / Section 301

21 U.S.C. § 301

Short title

Chapter 9 FEDERAL FOOD, DRUG, AND COSMETIC ACT / Subchapter I SHORT TITLE

Short title

Title 21 Title 21 / Section 379j–52

21 U.S.C. § 379j–52

Authority to assess and use biosimilar biological product fees

Part C Fees / Subpart 8 fees relating to biosimilar biological products

Authority to assess and use biosimilar biological product fees

Title 21 Title 21 / Section 379j

21 U.S.C. § 379j

Authority to assess and use device fees

Part C Fees / Subpart 3 fees relating to devices

Authority to assess and use device fees

Title 21 Title 21 / Section 379j–12

21 U.S.C. § 379j–12

Authority to assess and use animal drug fees

Part C Fees / Subpart 4 fees relating to animal drugs

Authority to assess and use animal drug fees

Title 21 Title 21 / Section 379j–21

21 U.S.C. § 379j–21

Authority to assess and use generic new animal drug fees

Part C Fees / Subpart 5 fees relating to generic new animal drugs

Authority to assess and use generic new animal drug fees

Title 21 Title 21 / Section 379j–22

21 U.S.C. § 379j–22

Reauthorization; reporting requirements

Part C Fees / Subpart 5 fees relating to generic new animal drugs

Reauthorization; reporting requirements

Title 21 Title 21 / Section 379j–41

21 U.S.C. § 379j–41

Definitions

Part C Fees / Subpart 7 fees relating to generic drugs

Definitions

Title 21 Title 21 / Section 379j–51

21 U.S.C. § 379j–51

Definitions

Part C Fees / Subpart 8 fees relating to biosimilar biological products

Definitions

Title 21 Title 21 / Section 379j–71

21 U.S.C. § 379j–71

Definitions

Part C Fees / Subpart 10 fees relating to over-the-counter drugs

Definitions

Title 21 Title 21 / Section 360ddd–2

21 U.S.C. § 360ddd–2

Inapplicability of drug fees to designated medical gases

Subchapter V DRUGS AND DEVICES / Part G Medical Gases

Inapplicability of drug fees to designated medical gases

Title 21 Title 21 / Section 393

21 U.S.C. § 393

Food and Drug Administration

Chapter 9 FEDERAL FOOD, DRUG, AND COSMETIC ACT / Subchapter X MISCELLANEOUS

Food and Drug Administration

Title 21 Title 21 / Section 399c

21 U.S.C. § 399c

Improving the training of State, local, territorial, and tribal food safety officials

Chapter 9 FEDERAL FOOD, DRUG, AND COSMETIC ACT / Subchapter X MISCELLANEOUS

Improving the training of State, local, territorial, and tribal food safety officials

Title 21 Title 21 / Section 352

21 U.S.C. § 352

Misbranded drugs and devices

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Misbranded drugs and devices

Title 21 Title 21 / Section 353

21 U.S.C. § 353

Exemptions and consideration for certain drugs, devices, and biological products

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Exemptions and consideration for certain drugs, devices, and biological products

Title 21 Title 21 / Section 355

21 U.S.C. § 355

New drugs

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

New drugs

Title 21 Title 21 / Section 360d

21 U.S.C. § 360d

Performance standards

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Performance standards

Title 21 Title 21 / Section 360e

21 U.S.C. § 360e

Premarket approval

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Premarket approval

Title 21 Title 21 / Section 360m

21 U.S.C. § 360m

Accredited persons

Subchapter V DRUGS AND DEVICES / Part A Drugs and Devices

Accredited persons