FDA Drug Approval
FDA Withdraws Approval of Amneal’s Celecoxib Capsule ANDA at Manufacturer’s Request
The U.S. Food and Drug Administration announced the withdrawal of approval for abbreviated new drug application (ANDA) 208833 covering Celecoxib capsules in 50 mg, 100 mg, 200 mg, and 400 mg strengths, which were held…
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