X
ACHEMA MIDDLE EAST
Pharma Advancement
DDF Summit
  • Home
  • Articles
  • Drug Development
    • All
    • Clinical Trials
    • FDA Approvals
    • Research & Development
    Bladder Cancer Treatment

    US FDA Approves Bladder Cancer Treatment Inlexzo from J&J

    Lilly TuneLab

    Eli Lilly Unveils Lilly TuneLab for AI-driven Drug Discovery

    Sensor Technology

    Enhancing Clinical Research with Advanced Sensor Technology

    Recombinant VWF

    FDA Approves Recombinant VWF Treatment in Pediatric Patients

    Novartis and Argo

    Novartis and Argo Signs Deal of up to $5.2b for Heart Drugs

    Novartis and Arrowhead

    Novartis and Arrowhead Sign Deal to Advance Parkinson’s Drug

    Eisais Leqembi IQLIK

    FDA Approves Eisai’s Leqembi IQLIK for Alzheimer’s Treatment

    FDA Approves Sanofis Wayrilz

    FDA Approves Sanofi’s Wayrilz for Immune Thrombocytopenia

    DAWNZERA for Hereditary Angioedema

    U.S. FDA Approves Ionis’ DAWNZERA for Hereditary Angioedema

  • Manufacturing
  • Supply Chain
  • Facilities
  • Insights
  • Events
  • Contact Us
No Result
View All Result
  • Home
  • Articles
  • Drug Development
    • All
    • Clinical Trials
    • FDA Approvals
    • Research & Development
    Bladder Cancer Treatment

    US FDA Approves Bladder Cancer Treatment Inlexzo from J&J

    Lilly TuneLab

    Eli Lilly Unveils Lilly TuneLab for AI-driven Drug Discovery

    Sensor Technology

    Enhancing Clinical Research with Advanced Sensor Technology

    Recombinant VWF

    FDA Approves Recombinant VWF Treatment in Pediatric Patients

    Novartis and Argo

    Novartis and Argo Signs Deal of up to $5.2b for Heart Drugs

    Novartis and Arrowhead

    Novartis and Arrowhead Sign Deal to Advance Parkinson’s Drug

    Eisais Leqembi IQLIK

    FDA Approves Eisai’s Leqembi IQLIK for Alzheimer’s Treatment

    FDA Approves Sanofis Wayrilz

    FDA Approves Sanofi’s Wayrilz for Immune Thrombocytopenia

    DAWNZERA for Hereditary Angioedema

    U.S. FDA Approves Ionis’ DAWNZERA for Hereditary Angioedema

  • Manufacturing
  • Supply Chain
  • Facilities
  • Insights
  • Events
  • Contact Us
No Result
View All Result
Pharma Advancement
No Result
View All Result
Home Asia

India’s drug industry to touch $48 billion by 2018

Yuvraj_pawp by Yuvraj_pawp
12th September 2014
in Asia, News

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

India’s drugs and pharmaceuticals industry is likely to post total sales of Rs.2.91 trillion ($47.88 billion) by 2018, with an average yearly growth of at least 14%, aided by a rapidly growing domestic market and the newly emerging export opportunity as patents of at least a dozen blockbuster drugs in the US expire in the next three years. 

“During 2014-2016, about $92 billion worth patented drugs are expected to go off patent in the US as compared with $65 billion during 2010-12,” says an industry analysis report released on Wednesday by Care Ratings, India’s second largest credit rating agency. The domestic drugs industry, which is valued at Rs.1.6 trillion at present, according to Care Ratings, is also expected to grow in the local market with aggressive rural penetration by drug makers, increased government spending on health and growing health awareness among people. 

The large number of drugs going off-patent in the US presents opportunities for local generic drug makers including Sun Pharmaceutical Industries Ltd, Lupin Ltd, Dr Reddy’s Laboratories Ltd and Cipla Ltd among others. 

Some of the important drugs whose patent will expire this year include Teva Pharmaceutical industries Ltd’s multiple sclerosis brand Capaxone, which had sales of $4.3 billion in 2013, AstraZeneca SA’s hyperacidity drug Nexium, which had sales of $3.9 billion, and Boehringer Ingelheim’s cardiac drug Micardis, which had sales of $2.2 billion. 

Anticipating the opportunity, Indian drug makers are building a strong pipeline of products to be sold in the US and have been filing abbreviated new drug applications (ANDA) to the US Food and Drug Administration (FDA), seeking approval for generic drugs. 

They can file ANDAs five years before the patent expiry date. ANDA is a process where generic drug makers seek approval for marketing the copycat version of patented drugs in the US, typically when the patent expires. Once the generic copies hit the market, the prices of these drugs fall, benefiting patients. Therefore, the government also encourages such filings. 

The US law allows a six-month exclusivity in the market to generic companies that file ANDAs first. 

During 2013, Indian companies secured approvals for 39% of the total 400 ANDAs filed. This is significantly higher than in 2012 when 37% of 476 such applications got approvals, according to the report. 

The domestic market will also see a significant growth in sales on the back of increasing affluence, changing lifestyles resulting in higher incidence of lifestyle-related diseases, increasing government expenditure on healthcare through schemes like the Central Government Health Scheme (CGHS), National Programme for Healthcare of the Elderly (NPHCE), Rashtriya Arogya Nidhi (RAN) and Janani Suraksha Yojana (JSY) in the next three years, according to Care analysis. 

Domestic consumption of drugs, which has grown on an average of 11% in the last five years, currently accounts for about 47% of the total local production, while 53% goes to export markets. 

The yearly average growth of drug exports in this period was 19%, which was also primarily driven by increasing demand for generics on the back of patent expiries of several high-value drugs such as Pfizer Inc.’s cardiac drug Lipitor, Roche’s Boniva, and GlaxoSmithKline Plc’s Combivir among others, according to Care Ratings report. 

India exports pharmaceutical products to more than 200 countries. But US, being the world’s largest generic drugs market, is the largest export market. However, the Care report also highlights risks of the increased regulatory concerns in the US market, which may hamper the revenue prediction for the industry. 

The US FDA has pulled up several major Indian drug exporters including Ranbaxy Laboratories Ltd, Sun Pharma and Wockhardt Ltd for non-compliance with quality standards in the local manufacturing units. Sun Pharma, the largest exporter of drugs to the US, had to stop exports from one of its manufacturing units in Gujarat in February and has been again put on alert as the US regulator has initiated a surprise inspection at another key unit in the state this week.

Tags: Asia Pacific
Previous Post

Spectrum Pharmaceuticals to Advance Neutropenia Drug

Next Post

Takeda and Lundbeck announce FDA approval of Brintellix™

Related Posts

misleading drug advertising
Facilities & Operation

US FDA Tightens Oversight on Misleading Drug Advertising

16th September 2025
Bladder Cancer Treatment
Drug Development

US FDA Approves Bladder Cancer Treatment Inlexzo from J&J

13th September 2025
Lilly TuneLab
Drug Development

Eli Lilly Unveils Lilly TuneLab for AI-driven Drug Discovery

12th September 2025
Recombinant VWF
Drug Development

FDA Approves Recombinant VWF Treatment in Pediatric Patients

9th September 2025
Novartis and Argo
Drug Development

Novartis and Argo Signs Deal of up to $5.2b for Heart Drugs

8th September 2025
Mod GRF 129 Peptide in scientific research
News

Mod GRF 1-29 Peptide: Investigating Its Potential in Scientific Research

8th September 2025
Next Post

Takeda and Lundbeck announce FDA approval of Brintellix™

Qucik Links

  • Drug Development
  • Manufacturing
  • News
  • Events & Conferences
  • Newsletter Archive
Pharma Advancement

About Us

Pharma Advancement is a leading Pharma information centric website. On one side Pharmaadvancement.com has established itself as one of the most efficient and comprehensive source of Pharma information online, dedicated to providing decision makers in all the Pharma industry sectors with reliable, accurate and useful insights into happenings in the Pharma sector.

Subscribe Us

System

  • Search
  • Sitemap
  • RSS Feed

Resources

  • Advertise with us
  • Contact Us
  • Download Mediapack
  • Newsletters Archive

© 2017 Copyright © Valuemediaservices 2017 All rights reserved.

No Result
View All Result
  • Home
  • Articles
  • Drug Development
  • Manufacturing
  • Supply Chain
  • Facilities
  • Insights
  • Events
  • Contact Us

© 2017 Copyright © Valuemediaservices 2017 All rights reserved.

Login to your account below

Forgotten Password?

Fill the forms bellow to register

All fields are required. Log In

Retrieve your password

Please enter your username or email address to reset your password.

Log In