Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 009112
Company: JOURNEY

Products on NDA 9112

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
EURAX	CROTAMITON	10%	LOTION;TOPICAL	Discontinued	None	Yes	No

Labels for NDA 009112

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
06/26/2003	SUPPL-21	Labeling	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2003/06927slr030,09112slr021_eurax_lbl.pdf