# 21 U.S.C. § 377: Revision of United States Pharmacopoeia; development of analysis and mechanical and physical tests

> Federal · Statutes · In force

URL: https://www.frixlaw.com/law-library/statutes/usc_t21_s377

## Section

- **Citation:** 21 U.S.C. § 377
- **Heading:** Revision of United States Pharmacopoeia; development of analysis and mechanical and physical tests
- **Jurisdiction:** Federal
- **Kind:** Statutes
- **Status:** In force
- **Text as of:** April 17, 2026
- **Source:** Publisher's official text
- **Location:** Title 21—FOOD AND DRUGS > CHAPTER 9—FEDERAL FOOD, DRUG, AND COSMETIC ACT > SUBCHAPTER VII—GENERAL AUTHORITY > Part A—General Administrative Provisions

## Text

The Secretary, in carrying into effect the provisions of the Federal Food, Drug, and Cosmetic Act [ 21 U.S.C. 301 et seq.], is authorized on and after July 12, 1943 , to cooperate with associations and scientific societies in the revision of the United States Pharmacopoeia and in the development of methods of analysis and mechanical and physical tests necessary to carry out the work of the Food and Drug Administration.

( July 12, 1943, ch. 221 , title II, 57 Stat. 500 ; 1953 Reorg. Plan No. 1, § 5, eff. Apr. 11, 1953 , 18 F.R. 2053, 67 Stat. 631 .)

## Nearby sections

- [21 U.S.C. § 371 Regulations and hearings](https://www.frixlaw.com/law-library/statutes/usc_t21_s371.md)
- [21 U.S.C. § 372 Examinations and investigations](https://www.frixlaw.com/law-library/statutes/usc_t21_s372.md)
- [21 U.S.C. § 372a Transferred](https://www.frixlaw.com/law-library/statutes/usc_t21_s372a.md)
- [21 U.S.C. § 373 Records](https://www.frixlaw.com/law-library/statutes/usc_t21_s373.md)
- [21 U.S.C. § 374 Inspection](https://www.frixlaw.com/law-library/statutes/usc_t21_s374.md)
- [21 U.S.C. § 374a Inspections relating to food allergens](https://www.frixlaw.com/law-library/statutes/usc_t21_s374a.md)
- [21 U.S.C. § 375 Publicity](https://www.frixlaw.com/law-library/statutes/usc_t21_s375.md)
- [21 U.S.C. § 376 Examination of sea food on request of packer; marking food with results; fees; penalties](https://www.frixlaw.com/law-library/statutes/usc_t21_s376.md)
- [21 U.S.C. § 377 Revision of United States Pharmacopoeia; development of analysis and mechanical and physical tests](https://www.frixlaw.com/law-library/statutes/usc_t21_s377.md)
- [21 U.S.C. § 378 Advertising of foods](https://www.frixlaw.com/law-library/statutes/usc_t21_s378.md)
- [21 U.S.C. § 379 Confidential information](https://www.frixlaw.com/law-library/statutes/usc_t21_s379.md)
- [21 U.S.C. § 379a Presumption of existence of jurisdiction](https://www.frixlaw.com/law-library/statutes/usc_t21_s379a.md)
- [21 U.S.C. § 379aa Serious adverse event reporting for nonprescription drugs](https://www.frixlaw.com/law-library/statutes/usc_t21_s379aa.md)
- [21 U.S.C. § 379aa–1 Serious adverse event reporting for dietary supplements](https://www.frixlaw.com/law-library/statutes/usc_t21_s379aa%E2%80%931.md)

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Source: Frix Law Library, https://www.frixlaw.com/law-library/statutes/usc_t21_s377. Check the current official text before relying on it. Not legal advice.
