Is CBD Legal in Brazil?
CBD is legal in Brazil only by prescription under ANVISA RDC 327/2019, with personal import via RDC 660/2022. No OTC sales. Full 2026 compliance guide.
CBD is legal in Brazil only by prescription under ANVISA RDC 327/2019, with personal import via RDC 660/2022. No OTC sales. Full 2026 compliance guide.
CBD is legal in Brazil only through medical channels regulated by ANVISA. The framework rests on RDC 327/2019, which created the Cannabis Product category and a five-year Sanitary Authorization for manufacture, import, prescription, and dispensing through licensed pharmacies. Authorized products must contain predominantly CBD; products with more than 0.2% THC are restricted to terminally ill or treatment-refractory patients. There is no over-the-counter or wellness CBD market.
Patients who cannot access ANVISA-authorized products domestically may import CBD for personal use under RDC 660/2022. Patients or their legal representatives register through the gov.br portal, upload a valid medical prescription, and obtain an exceptional import authorization valid for up to two years. About 47% of Brazilian medical cannabis patients still rely on this personal-import route. Habeas corpus rulings have also allowed select patients to cultivate at home for medicinal use. Mevatyl (nabiximols) remains the only fully registered cannabis-based medicine, approved in January 2017 for multiple sclerosis spasticity.
This page is for informational purposes only and does not constitute legal advice. Verify current law with qualified counsel before making compliance decisions.
Medical Only
Agência Nacional de Vigilância Sanitária (ANVISA)
Predominantly CBD; products with >0.2% THC restricted to terminal or refractory patients
ANVISA RDC 327/2019; RDC 660/2022
Personal import is permitted under RDC 660/2022 with a valid prescription from a licensed Brazilian physician and prior registration with ANVISA via the gov.br portal. Authorizations are valid for up to two years and allow shipment of finished products from foreign manufacturers regularized in their country of origin. Commercial import for resale requires RDC 327/2019 Sanitary Authorization, an Operating License (AFE), Special Authorization (AE), and GMP certification.