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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 203299
Company: HIKMA
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
BIMATOPROST BIMATOPROST 0.03% SOLUTION/DROPS;OPHTHALMIC Discontinued None No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
11/08/2018 ORIG-1 Approval

Label is not available on this site.

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