Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 019356
Company: LEGACY

Products on NDA 19356

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
NAFTIN	NAFTIFINE HYDROCHLORIDE	1%	GEL;TOPICAL	Discontinued	None	Yes	No

Labels for NDA 019356

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
04/30/2018	SUPPL-8	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/019356s008,019599s014,204286s003lbl.pdf