Home
Menu
Call attorney Graham Syfert at 904-383-7448
Personal Injury Lawyer
Florida Statute 465.0251 | Lawyer Caselaw & Research
F.S. 465.0251 Case Law from Google Scholar
Statute is currently reporting as:
Link to State of Florida Official Statute Google Search for Amendments to 465.0251

The 2023 Florida Statutes (including Special Session C)

Title XXXII
REGULATION OF PROFESSIONS AND OCCUPATIONS
Chapter 465
PHARMACY
View Entire Chapter
F.S. 465.0251
465.0251 Generic drugs; removal from formulary under specified circumstances.
(1) The Board of Pharmacy and the Board of Medicine shall remove any generic named drug product from the formulary established by s. 465.025(6), if every commercially marketed equivalent of that drug product is “A” rated as therapeutically equivalent to a reference listed drug or is a reference listed drug as referred to in “Approved Drug Products with Therapeutic Equivalence Evaluations” (Orange Book) published by the United States Food and Drug Administration.
(2) Nothing in this act shall alter or amend s. 465.025 as to existing law providing for the authority of physicians to prohibit generic drug substitution by writing “medically necessary” on the prescription.
History.ss. 1, 2, ch. 2001-146.

F.S. 465.0251 on Google Scholar

F.S. 465.0251 on Casetext

Amendments to 465.0251


Arrestable Offenses / Crimes under Fla. Stat. 465.0251
Level: Degree
Misdemeanor/Felony: First/Second/Third

Current data shows no reason an arrest or criminal charge should have occurred directly under Florida Statute 465.0251.



Annotations, Discussions, Cases:

Cases from cite.case.law:

ABBOTT LABORATORIES, v. MYLAN PHARMACEUTICALS, INC., 15 So. 3d 642 (Fla. Dist. Ct. App. 2009)

. . . Section 465.0251(1) removes a generic drug from the NDF if the generic drug is “A” rated as therapeutically . . . Because the ALJ erred in interpreting section 465.0251(1) to apply to editions of the Orange Book subsequent . . . Section 465.0251, Florida Statutes (2007), permits removal from the NDF under specific circumstances . . . Although subsection (1) of section 465.0251 requires removal of a drug product from the NDF without an . . . Section 165.0251 We now turn to the merits of the parties’ arguments with respect to section 465.0251 . . .