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India

Centre proposes strict curbs on advertising prescription drugs including GLP-1 medicines

The proposed amendment will also cover GLP-1-based drugs and related dual agonists like Mounjaro, Ozempic, and Wegovy, all prescription medications that manage type 2 diabetes and chronic weight management.

Kavita Bajeli-Datt

NEW DELHI: The centre has proposed strict curbs on advertising of prescription drugs by retailers and wholesalers. The move aims to curb unauthorised promotion of prescription medicines and strengthen safeguards for public health.

The proposed amendment to the Drugs Rules, 1945, seeks to extend existing restrictions on advertisements of Schedule H, H1 and X medicines to drug retailers, wholesalers and distributors.

The amendment will also cover GLP-1-based drugs and related dual agonists like Mounjaro, Ozempic, and Wegovy, all prescription medications that manage type 2 diabetes and chronic weight management.

In recent times, pharmacies have advertised these ‘blockbuster medicines’ and even offered discounts as these drugs have become widely used for weight management. However, no action could be taken against them.

Now, the proposed measure is expected to reinforce safeguards relating to medicines that require appropriate medical supervision, which also include certain antibiotics, psychotropic medicines and other prescription-only drugs.

Officials said the Union Ministry of Health and Family Welfare has proposed the amendment to the Drugs Rules, 1945, to strengthen regulation of advertisements relating to prescription-only medicines.

The draft amendment has been notified through Gazette Notification G.S.R. 861(E), dated September 28, 2026, following consultations with the Drugs Technical Advisory Board (DTAB).

Under the existing regulatory framework, pharmaceutical manufacturers are prohibited from advertising drugs covered under Schedule H, Schedule H1 and Schedule X without prior sanction of the central government.

However, corresponding provisions have not explicitly covered entities engaged in the retail and wholesale sale and distribution of these medicines.

To address this regulatory gap, the ministry has proposed the insertion of sub-rule (22) under Rule 65 of the Drugs Rules, 1945, extending the advertisement restriction to holders of licences to sell, stock, exhibit or offer for sale, or distribute drugs, including retail and wholesale drug licence holders.

Under the proposed provision, no advertisement of drugs specified in Schedule H, Schedule H1 or Schedule X shall be made except with the previous sanction of the central government.

The proposed amendment is intended to strengthen regulatory oversight across the pharmaceutical supply chain, discourage unauthorised promotion of prescription medicines and reduce risks associated with inappropriate self-medication.

The proposal follows the recommendations of the 93rd meeting of the Drugs Technical Advisory Board, held on February 16, 2026, which considered the need for appropriate provisions governing advertisements by drug sale and distribution licence holders.

The ministry has invited objections and suggestions from stakeholders and members of the public within 30 days from the date on which copies of the gazette containing the draft rules are made available to the public.

Officials said submissions received within the prescribed period will be considered by the central government before finalisation of the amendment.

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