Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 021114
Company: ALCON PHARMS LTD

Products on NDA 21114

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
BETAXON	LEVOBETAXOLOL HYDROCHLORIDE	EQ 0.5% BASE	SUSPENSION/DROPS;OPHTHALMIC	Discontinued	None	No	No

Labels for NDA 021114

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
03/09/2010	SUPPL-3	Labeling	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/021114s003lbl.pdf
02/23/2000	ORIG-1	Approval	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2000/21114lbl.pdf