SAFE Drugs Act of 2025

(1) by amending paragraph (1)(D) to read as follows:

(D) does not, more than 20 times in a single month, compound any drug product that is essentially a copy of a commercially available drug product.

(1) ; and

(2) by amending paragraph (2) to read as follows:

(A) For purposes of paragraph (1)(D), the term essentially a copy of a commercially available drug product means any drug product—

(i) that contains any active ingredient found in a commercially available drug product; and

(ii) in which there is no change, made for an identified individual patient, which produces for that patient a significant difference, as determined by the prescribing practitioner, between the compounded drug product and the comparable commercially available drug product.

(B) For purposes of subparagraph (A), the term commercially available drug product includes any drug product that—

(i) is sold in the commercial marketplace in the United States and manufactured in one or more facilities required to comply with section 501(a)(2)(B); and

(ii) is not included in the discontinued section of the list of products described in section 505(j)(7)(A).

(1) by redesignating subsections (d) and (e) as subsections (e) and (f), respectively; and

(2) by inserting after subsection (c) the following:

For calendar year 2025 and each calendar year thereafter, if a pharmacy, facility, or physician compounds, more than 20 times in a single month for patients who reside outside the State in which the compounding occurs, any drug product that contains any active ingredient found in a commercially available drug product (as defined in subsection (b)(2)(B)), such pharmacy, facility, or physician shall submit a report to the Secretary.

Each report under paragraph (1) shall identify—

(A) each type of drug product described in paragraph (1) that is compounded for a patient described in such paragraph; and

(B) for each month, the total number of times each such type is so compounded.

For any calendar year for which paragraph (1) applies, the pharmacy, facility, or physician shall submit the report under such paragraph not later than the end of such calendar year.

A pharmacy, facility, or physician shall submit each report under paragraph (1) in such form and manner as the Secretary may prescribe.

This subsection does not apply to the compounding of any drug products for hospital patients by a pharmacy located on the premises of the hospital.

Section 503B(b) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 353b(b)) is amended by adding at the end the following:

In the case of a large-scale outsourcing facility, the risk-based inspections under paragraph (4) shall include—

(i) an inspection prior to such facility compounding any drug product for the first time; and

(ii) the reinspection of such facility not less than biennially.

For purposes of this paragraph, the term large-scale outsourcing facility means any outsourcing facility that compounds, more than 100 times in a single calendar year, any drug product.

Section 510(g)(1) of such Act (21 U.S.C. 360(g)(1)) is amended by inserting before the semicolon at the end the following:, except that the exemption in this paragraph shall not apply to any outsourcing facility (as defined in section 503B(d)(4)).

The amendments made by subsections (a) and (b) apply beginning 6 months after the date of enactment of this Act.