Animal Drug User Fee Amendments of 2008

Pub. L. 110–316

Also known as: Animal Generic Drug User Fee Act of 2008

US Codex doesn’t hold the enacted text of this law — the public-law corpus runs from the 113th Congress (2013) onward. What it changed in the U.S. Code, reconstructed from the credit notes, is listed below.

16 sections of the Code credited to this law, found between Public Law 110-180 and Public Law 110-460.

• 21 U.S.C. § 355 — New drugs
• 21 U.S.C. § 360b — New animal drugs
• 21 U.S.C. § 379j-11 — 379j–11. Definitions
• 21 U.S.C. § 379j-12 — 379j–12. Authority to assess and use animal drug fees
• 21 U.S.C. § 379j-13 — 379j–13. Reauthorization; reporting requirements
• 21 U.S.C. § 379j-21 — 379j–21. Authority to assess and use generic new animal drug fees
• 21 U.S.C. § 379j-22 — 379j–22. Reauthorization; reporting requirements
• 21 U.S.C. § 379k — Information system
• 21 U.S.C. § 379l — Education
• 21 U.S.C. § 379o — Environmental impact
• 42 U.S.C. § 282 — Director of National Institutes of Health
• 21 U.S.C. § 379j–11 — Definitions
• 21 U.S.C. § 379j–12 — Authority to assess and use animal drug fees
• 21 U.S.C. § 379j–13 — Reauthorization; reporting requirements
• 21 U.S.C. § 379j–21 — Authority to assess and use generic new animal drug fees
• 21 U.S.C. § 379j–22 — Reauthorization; reporting requirements