California Health and Safety Code

§ 127691

HSC § 127691 Effective Jul 10, 2023Div. 107 · Part 2 · Ch. 10

Statute text

For purposes of this chapter, the following definitions apply:

(a)“Generic drug” means a drug that is approved pursuant to subdivision (j) of Section 355 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. Sec. 301 et seq.), or a biosimilar, as defined under the federal Public Health Service Act (42 U.S.C. Sec. 262).

(b)“Partnerships” include, but are not limited to, agreements for the procurement of generic prescription drugs by way of contracts, grant agreements, or purchasing by a payer, state governmental agency, group purchasing organization, nonprofit organization, or other entity.

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Legislative history

Amended by Stats. 2023, Ch. 42, Sec. 50. (AB 118) Effective July 10, 2023.