Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 017703
Company: ABBOTT

• Other Important Information from FDA

Products on NDA 17703

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
CYLERT	PEMOLINE	37.5MG	TABLET, CHEWABLE;ORAL	Discontinued	None	No	No

Labels for NDA 017703

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
11/21/2003	SUPPL-18	Labeling	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2003/016832s022_017703s018lbl.pdf