On 15 May 2013, India’s Directorate of Food and Drugs Administration announced the introduction of a new Drug Price Control Order (DPCO), which is expected to lead to price reductions of up to 80% in ‘essential drugs’.
India introduces new drug pricing control
Home/Policies & Legislation | Posted 31/05/2013 0 Post your comment
The new DPCO, which affects both brand-name and generic drugs, replaces the 1995 Order which was based on production costs for drugs and regulated the prices of just 74 active pharmaceutical ingredients (APIs) and their finished formulations in the country’s National List of Essential Medicines [1].
The government will now regulate the rates of 652 medicines using a market price-linked cap for each drug. The DPCO proposes that the retail price of 348 ‘essential drugs’ be fixed at the simple average price of brands that have more than 1% market share.
The maximum retail price of a drug will also include a margin of 16% for the pharmacist. The prices prevailing in May 2012 will be taken as the reference point for calculating the caps. Drug producers will be permitted an annual increase in the retail price in line with the wholesale price index.
Companies selling medicines above the government-mandated ceiling rates will have to reduce prices to conform to the new rules, but those selling drugs below the ceiling price will not be allowed to raise their prices. Firms that launch new medicines can sell them at or below government-set price caps.
Existing firms will also not be allowed to stop production of a drug without permission from the government. Firms will have to issue a public notice and inform the Indian Government at least six months in advance if they want to stop making an essential drug and the government can ask them to continue producing the drug at a certain level for another year if in the public interest.
The National Pharmaceuticals Pricing Authority (NPPA) will implement the new DPCO, which will come into effect on 1 July 2013. The implementation of the new DPCO is expected to lead to reductions of 50–80% in the prices of many life-saving anticancer and anti-infective drugs.
Related articles
India supplies 20% of generic drugs worldwide
India issues more compulsory licences
Reference
1. GaBI Online - Generics and Biosimilars Initiative. India may move away from compulsory licensing [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2013 May 31]. Available from: www.gabionline.net/Generics/General/India-may-move-away-from-compulsory-licensing
Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.
Copyright – Unless otherwise stated all contents of this website are © 2013 Pro Pharma Communications International. All Rights Reserved.
Source: DFDA
Guidelines
Regulatory update for post-registration of biological products in Brazil
New regulations in Brazil for the registration of biosimilars
Reports
Top nine biological drugs by sales in 2023
New findings of semaglutide in managing hidradenitis suppurativa
Most viewed articles
The best selling biotechnology drugs of 2008: the next biosimilars targets
Global biosimilars guideline development – EGA’s perspective
Comments (0)
Post your comment