Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 020706
Company: NOVARTIS

Products on NDA 20706

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
EMADINE	EMEDASTINE DIFUMARATE	0.05%	SOLUTION/DROPS;OPHTHALMIC	Discontinued	None	Yes	No

Labels for NDA 020706

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
05/12/2003	SUPPL-11	Labeling	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2003/20706slr011_emadine_lbl.pdf