Search the current U.S. Code within Title 21

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11 results 379aa-1

Scoped to Title 21

Exact match Title 21 Title 21 / Chapter 9 FEDERAL FOOD, DRUG, AND COSMETIC ACT / Subchapter VII GENERAL AUTHORITY / Part H Serious Adverse Event Reports / Section 379aa–1

21 U.S.C. § 379aa–1

Serious adverse event reporting for dietary supplements

Subchapter VII GENERAL AUTHORITY / Part H Serious Adverse Event Reports

Exact citation match for 21 USC § 379AA-1

Title 21 Title 21 / Section 2110

21 U.S.C. § 2110

Rule of construction

Chapter 26 FOOD SAFETY

Rule of construction

Title 21 Title 21 / Section 343

21 U.S.C. § 343

Misbranded food

Chapter 9 FEDERAL FOOD, DRUG, AND COSMETIC ACT / Subchapter IV FOOD

Misbranded food

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 331

21 U.S.C. § 331

Prohibited acts

Chapter 9 FEDERAL FOOD, DRUG, AND COSMETIC ACT / Subchapter III PROHIBITED ACTS AND PENALTIES

Prohibited acts

Title 21 Title 21 / Section 350g

21 U.S.C. § 350g

Hazard analysis and risk-based preventive controls

Chapter 9 FEDERAL FOOD, DRUG, AND COSMETIC ACT / Subchapter IV FOOD

Hazard analysis and risk-based preventive controls

Title 21 Title 21 / Section 381

21 U.S.C. § 381

Imports and exports

Chapter 9 FEDERAL FOOD, DRUG, AND COSMETIC ACT / Subchapter VIII IMPORTS AND EXPORTS

Imports and exports

Title 21 Title 21 / Section 379aa

21 U.S.C. § 379aa

Serious adverse event reporting for nonprescription drugs

Subchapter VII GENERAL AUTHORITY / Part H Serious Adverse Event Reports

Serious adverse event reporting for nonprescription drugs

Title 21 Title 21 / Section 379j–73

21 U.S.C. § 379j–73

Reauthorization; reporting requirements

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

Reauthorization; reporting requirements

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