Zydus Cadila has received final approval from the US Food and Drug Administration (USFDA) to market Tranexamic acid injection in the strength of 1,000mg/10 mL (100mg/mL) single dose vial, Cadila Healthcare said in a BSE filing.
The product will be produced at the group's formulations manufacturing facility at Moraiya in Ahmedabad, it added.
Also Read
The Gujarat-based group has more than 130 approvals and has so far filed over 300 abbreviated new drug applications (ANDAs).
Shares of Cadila Healthcare, the listed entity of the Zydus group today closed 3.68 per cent higher at Rs 544.25 per scrip on BSE.
(Only the headline and picture of this report may have been reworked by the Business Standard staff; the rest of the content is auto-generated from a syndicated feed.)
You’ve reached your limit of {{free_limit}} free articles this month.
Subscribe now for unlimited access.
Already subscribed? Log in
Subscribe to read the full story →
Smart Quarterly
₹900
3 Months
₹300/Month
Smart Essential
₹2,700
1 Year
₹225/Month
Super Saver
₹3,900
2 Years
₹162/Month
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
)