FDA Drug Approval, A205894, CYCLOSPORINE

FDA Drug Approval, A205894, CYCLOSPORINE

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ANDA: 205894
Company: MYLAN
Drug Name: CYCLOSPORINE
Active Ingredients: CYCLOSPORINE
Strength: 0.05%
Dosage Form/Route: EMULSION;OPHTHALMIC
Action Date: 02/02/2022
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB
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