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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 205975
Company: TARO
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
NAFTIFINE HYDROCHLORIDE NAFTIFINE HYDROCHLORIDE 1% CREAM;TOPICAL Prescription None No Yes
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
09/08/2016 ORIG-1 Approval STANDARD

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
12/03/2019 SUPPL-1 Labeling-Package Insert

Label is not available on this site.

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