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  1. LII
  2. Electronic Code of Federal Regulations (e-CFR)
  3. Title 40—Protection of Environment
  4. CHAPTER I—ENVIRONMENTAL PROTECTION AGENCY
  5. SUBCHAPTER N—EFFLUENT GUIDELINES AND STANDARDS
  6. PART 439—PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY

40 CFR Part 439 - PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY

  • CFR
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  1. General (§§ 439.0 - 439.4)
    1. § 439.0 Applicability.
    2. § 439.1 General definitions.
    3. § 439.2 General monitoring requirements.
    4. § 439.3 General pretreatment standards.
    5. § 439.4 General limitation or standard for pH.
  2. Subpart A—Fermentation Products (§§ 439.10 - 439.17)
  3. Subpart B—Extraction Products (§§ 439.20 - 439.27)
  4. Subpart C—Chemical Synthesis Products (§§ 439.30 - 439.37)
  5. Subpart D—Mixing/Compounding and Formulation (§§ 439.40 - 439.47)
  6. Subpart E—Research (§§ 439.50 - 439.52)
  7. SUBPART (§§ - )
  8. Appendix A to Part 439—Tables
Authority:
33 U.S.C. 1311, 1314, 1316, 1317, 1318, 1342 and 1361.
Source:
48 FR 49821, Oct. 27, 1983, unless otherwise noted.

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