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Concord Biotech gets FDA-approval for Tofacitinib tablets

10 Jun 2026via NSE FilingSource

Concord Biotech gets FDA-approval for Tofacitinib tablets — Concord Biotech has received abbreviated new drug application (ANDA) approval from the US FDA for Tofacitinib Tablets, 5 mg and 10 mg, paving the way for market entry. The drug is a generic version of Xeljanz, used to treat rheumatoid arthritis and other inflammatory conditions. This approval expands Concord Biotech’s presence in the US generics market.
📊 STOCKS: CONCORDBIO | 🏢 SECTOR: Pharma | #MEDIUMIMPACT #FDAApproval

#FDAApproval#GenericDrug#ANDA

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⚠️ This brief is AI-generated from public news sources for informational purposes only. Not investment advice. Always consult a SEBI-registered advisor before trading.

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