All regulations
Nonrulemaking
FDA
Open for Comments
FDA-2026-P-2641
Requests that the FDA remove from the market the injectable contraceptive Depot Medroxyprogesterone Acetate (DMPA; Depo Provera) based on conclusive evidence that it uniquely facilitates the transmission of HIV from men to women and has other known risks. Numerous alternatives are available.
Documents
38
Comments
0
Key Dates
Comment Period OpensMar 13, 2026
Documents
| Type | Title | Status |
|---|---|---|
Supporting Material |
Keywords
CDER
Citizen Petition
Contraceptive Study Group
remove from the
market the injectable contraceptive
Depot Medroxyprogesterone Acetate
DMPA
Depo Provera
based on
Data from Regulations.gov