The Directorate General of Drug Administration (DGDA) is the regulatory body responsible for overseeing the manufacture, registration, and quality of medicines — including Unani, Ayurvedic, and Unani-Ayurvedic-Herbal formulations — in Bangladesh.
A DGDA-registered product has gone through a formal review process, including documentation of its formulation, manufacturing process, and compliance with national drug administration standards, before it can legally be sold.
Every Bengal Laboratories product carries a unique D.A.R (Drug Administration Registration) number, which can be referenced on the product’s packaging and on its product page on this website.
This registration is separate from, and in addition to, our GMP (Good Manufacturing Practice) certification, which governs the conditions and processes inside our manufacturing facility.
Together, DGDA registration and GMP certification are two of the clearest indicators that a Unani product is manufactured to a verifiable, regulated standard — something we encourage every patient and distributor to check for when choosing a Unani medicine brand.
