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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 091034
Company: ZAMBON SPA
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
DORZOLAMIDE HYDROCHLORIDE DORZOLAMIDE HYDROCHLORIDE EQ 2% BASE 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
12/04/2013 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
04/06/2015 SUPPL-1 Labeling-Package Insert

Label is not available on this site.

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