Concord Biotech Limited has made a milestone achievement with the United States Food and Drug Administration (USFDA) approving marketing its Teriflunomide tablets. The approvals are for the 7 mg and 14 mg strengths, making Concord Biotech a significant player in managing relapsing forms of multiple sclerosis (MS). Teriflunomide is a pyrimidine synthesis inhibitor that decreases flare-ups and delays the progression of physical symptoms in MS patients.
Key Highlights:
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Therapeutic Impact: Teriflunomide tablets are used to treat relapsing forms of MS, such as clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease.
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Manufacturing Excellence: Concord Biotech's facilities have met stringent USFDA requirements, which means they comply with current good manufacturing practices (cGMP).
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Market Opportunity: The approval provides access to the high-value US market, where the demand for effective MS treatments remains on the rise.
This approval reflects Concord Biotech's dedication 85lakhs to driving global healthcare solutions and is another milestone in its path of innovation and excellence. With this success, the company is set to increase its presence in the pharmaceutical sector while making a positive impact on patient outcomes.
Source: Pharma Industrial India