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TWi Biotechnology receives approval of protocol for its drug AC-201 Controlled-Release Tablet, Phase II clinical trial in both the United States and Taiwan
TWi Pharmaceuticals Receives US FDA Approval on Generic Donepezil Hydrochloride Tablets USP, 23 mg, its fifth ANDA from US FDA
TWi Biotechnology Receives Orphan Drug Designation for its Lead Drug Candidate AC-201 in United States.
TWi Pharmaceuticals Receives US FDA Final Approval on Generic Megestrol Acetate 125mg/ml Oral Suspension
TWi Biotechnology Receives Notice of Patent Allowance for Its Lead Drug Candidate AC-201 in United States.
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