CSIMarket
 
Ironwood Pharmaceuticals inc   (NASDAQ: IRWD)
 

Ironwood Pharmaceuticals Inc's Customers Performance

IRWD



 
IRWD's Source of Revenues During the corresponding time, Ironwood Pharmaceuticals Inc recorded a revenue increase by 32.62 % year on year, sequentially revenue grew by 6.14 %. While revenue at the Ironwood Pharmaceuticals Inc 's corporate clients

List of IRWD Customers




for the same period Ironwood Pharmaceuticals Inc recorded revenue increase by 32.62 % year on year, sequentially revenue grew by 6.14 %.

List of IRWD Customers

Ironwood Pharmaceuticals Inc's Business Units
North America    191.1 % of total Revenue
Europe and Other    1.7 % of total Revenue
Collaborative Arrangement Collaboration and License Agreements    0.14 % of total Revenue
Canada and Mexico    1.59 % of total Revenue
Royalty    0.18 % of total Revenue
Royalty Canada and Mexico AbbVie Plc    0.62 % of total Revenue






Ironwood Pharmaceuticals Inc's Comment on Sales, Marketing and Customers



The Hatch-Waxman Act establishes the regulatory framework for marketing and distributing generic drugs in the United States. It permits generic drug manufacturers to submit abbreviated new drug applications (ANDAs) to the U.S. Food and Drug Administration (FDA), relying on prior safety and effectiveness data of brand-name drugs. The Act grants market exclusivity periods to encourage drug development, including five years for new chemical entities and three years for certain new clinical investigations related to approved drugs. These exclusivity periods prevent approval of competing generic drugs for specified conditions during the protected timeframe. Additionally, new drug application (NDA) applicants must provide patent information for listing in the FDA's Orange Book, and ANDA or 505(b)(2) applicants are required to submit certifications concerning these patents.





Ironwood Pharmaceuticals Inc’s Comment on Sales, Marketing and Customers


The Hatch-Waxman Act establishes the regulatory framework for marketing and distributing generic drugs in the United States. It permits generic drug manufacturers to submit abbreviated new drug applications (ANDAs) to the U.S. Food and Drug Administration (FDA), relying on prior safety and effectiveness data of brand-name drugs. The Act grants market exclusivity periods to encourage drug development, including five years for new chemical entities and three years for certain new clinical investigations related to approved drugs. These exclusivity periods prevent approval of competing generic drugs for specified conditions during the protected timeframe. Additionally, new drug application (NDA) applicants must provide patent information for listing in the FDA's Orange Book, and ANDA or 505(b)(2) applicants are required to submit certifications concerning these patents.








IRWD's vs. Customers, Data

(Revenue and Income for Trailing 12 Months, in Millions of $, except Employees)



COMPANY NAME MARKET CAP REVENUES INCOME EMPLOYEES
Ironwood Pharmaceuticals inc 685.43 361.51 102.18 100
SUBTOTAL 0.00 0.00 0.00 -

Sources: Ironwood Pharmaceuticals inc’s official press releases and regulatory filings; CSIMarket.com’s market research; and the financial filings and press releases of other companies cited in this report.
Updated on:
Focus of this report: Ironwood Pharmaceuticals inc’s corporate clients.
For your research, we’ve provided 9 tables on Ironwood Pharmaceuticals inc corporate clients.
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