Tap any paragraph to write a margin note. Your notes collect in the Desk below the text and file under cases with @. The side-by-side margin rail opens on a larger screen.

Code · STATUTE-COMPILATIONS · FDA Reauthorization Act of 2017 · Sec. 808

Sec. 808. INCENTIVIZING COMPETITIVE GENERIC DRUG DEVELOPMENT

435 words·~2 min read·/statute-compilations/comps-15234/sec-808

A research copy — for the controlling text, always check the official state or federal source. Not legal advice.

## SEC. 808 INCENTIVIZING COMPETITIVE GENERIC DRUG DEVELOPMENT Section 505(j)(5) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355(j)(5)) is amended— ####
(1)in subparagraph (B), by adding at the end the following: > > ###### “(v) 180-day exclusivity period for competitive generic therapies > > > ###### “(I) Effectiveness of application > > Subject to subparagraph (D)(iv), if the application is for a drug that is the same as a competitive generic therapy for which any first approved applicant has commenced commercial marketing, the application shall be made effective on the date that is 180 days after the date of the first commercial marketing of the competitive generic therapy (including the commercial marketing of the listed drug) by any first approved applicant. > > > ###### “(II) Limitation > > The exclusivity period under subclause
(I)shall not apply with respect to a competitive generic therapy that has previously received an exclusivity period under subclause (I). > > > ###### “(III) Definitions > > In this clause and subparagraph (D)(iv): > > > ###### “(aa) > > The term ‘competitive generic therapy’ means a drug— > > > ###### “(AA) > > that is designated as a competitive generic therapy under section 506H; and > > > ###### “(BB) > > for which there are no unexpired patents or exclusivities on the list of products described in section 505(j)(7)(A) at the time of submission. > > > ###### “(bb) > > The term ‘first approved applicant’ means any applicant that has submitted an application that— > > > ###### “(AA) > > is for a competitive generic therapy that is approved on the first day on which any application for such competitive generic therapy is approved; > > > ###### “(BB) > > is not eligible for a 180-day exclusivity period under clause
(iv)for the drug that is the subject of the application for the competitive generic therapy; and > > > ###### “(CC) > > is not for a drug for which all drug versions have forfeited eligibility for a 180-day exclusivity period under clause
(iv)pursuant to subparagraph (D).” > ; and ####
(2)in subparagraph (D), by adding at the end the following: > > ###### “(iv) Special forfeiture rule for competitive generic therapy > > The 180-day exclusivity period described in subparagraph (B)(v) shall be forfeited by a first approved applicant if the applicant fails to market the competitive generic therapy within 75 days after the date on which the approval of the first approved applicant’s application for the competitive generic therapy is made effective.” > .
Connectionstraces to 1
Traces to 1 document
Citation graph
cites case law
Sec. 808
INCENTIVIZING COMPETITIVE GENERIC DRUG DEVELOPMENT
Cites 1Cited by 0 across 0 sources
★   the supreme law of the land   ★
Don't Tread on Me
E Pluribus Unum — out of many, one

"If you don't know your rights, you don't have any."

Marginalia · a citizen's law index
A research desk, not legal advice. Always read the cited source before relying on a summary.
Questions or an issue? support@self-law.org
disclaimerMarginalia is a research index, not a law firm. Nothing on this site is legal, tax, or financial advice and no attorney–client relationship is formed by using it. Statutes, regulations, and case law change; summaries, search results, AI output, and member posts may be incomplete, out of date, or wrong. Any interpretation drawn from material on this site should be validated by a licensed attorney in your jurisdiction before you act on it.