Indian drugmakers may have to cough up higher facility fee

The US laws authorise the drug and health watchdog to assess and collect user fees for certain applications and supplements for human generic drug products

Press Trust of India Washington
Last Updated : Aug 04 2014 | 2:20 AM IST
Drugmakers from India, the biggest source of medicines to the US, may soon have to cough up 12-15 per cent more in annual facility fees as the Food and Drug Administration (FDA) has announced new rates. The US laws authorise the drug and health watchdog to assess and collect user fees for certain applications and supplements for human generic drug products.

The new rates, applicable on companies from all nations, are effective from October 1 and will remain in force through September 30, 2015, according to  communication from FDA.

A foreign FDF (finished dosage form) facility will pay $262,717 (approximately Rs 1.6 crore) now compared to $235,152 a year ago — an increase of 12 per cent. India is home to over 150 FDA-approved plants, including facilities run by global MNCs. Of the total facilities identified as FDF, there were 271 domestic facilities and 410 foreign facilities, including those in India.

Similarly, a foreign API (active pharmaceutical ingredient) facility would attract $56,926 (about Rs 34.7 lakh) as fees — 15 per cent higher than the current rate. Of the total facilities identified as API facilities, there were 103 domestic facilities and 692 foreign facilities.

Facility fees are required to be paid by those owning a facility, which is identified or intended to be identified in at least one generic drug submission that is pending or approved to produce one or more generic drug FDFs and/or APIs. If a facility manufactures both generic FDFs and APIs, it incurs both annual FDF and annual API facility fees. Foreign generic drug facility fees are about $15,000 higher than domestic plants as FDA reasons the differential reflects the additional costs of inspections funded. For the US facilities, the FDF facility fee this year is $247,717 and the API facility fee is $41,926.

Interestingly, the total FDF and API fees collected from domestic as well as foreign facilities account for 70 per cent of the $312 million target fee revenue amount for FY 2015. This is why, industry players say, the cut in filing fees this year provides little relief.The new fee for drug master files (DMFs) is $26,720 (approximately Rs 16.3 lakh), down 15 per cent year-on-year.
*Subscribe to Business Standard digital and get complimentary access to The New York Times

Smart Quarterly

₹900

3 Months

₹300/Month

SAVE 25%

Smart Essential

₹2,700

1 Year

₹225/Month

SAVE 46%
*Complimentary New York Times access for the 2nd year will be given after 12 months

Super Saver

₹3,900

2 Years

₹162/Month

Subscribe

Renews automatically, cancel anytime

Here’s what’s included in our digital subscription plans

Exclusive premium stories online

  • Over 30 premium stories daily, handpicked by our editors

Complimentary Access to The New York Times

  • News, Games, Cooking, Audio, Wirecutter & The Athletic

Business Standard Epaper

  • Digital replica of our daily newspaper — with options to read, save, and share

Curated Newsletters

  • Insights on markets, finance, politics, tech, and more delivered to your inbox

Market Analysis & Investment Insights

  • In-depth market analysis & insights with access to The Smart Investor

Archives

  • Repository of articles and publications dating back to 1997

Ad-free Reading

  • Uninterrupted reading experience with no advertisements

Seamless Access Across All Devices

  • Access Business Standard across devices — mobile, tablet, or PC, via web or app

More From This Section

First Published: Aug 04 2014 | 12:19 AM IST

Next Story