Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 021712
Company: UCB INC

Products on NDA 21712

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
FLUXID	FAMOTIDINE	20MG	TABLET, ORALLY DISINTEGRATING;ORAL	Discontinued	None	No	No
FLUXID	FAMOTIDINE	40MG	TABLET, ORALLY DISINTEGRATING;ORAL	Discontinued	None	No	No

Labels for NDA 021712

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
09/24/2004	ORIG-1	Approval	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2004/21712lbl.pdf