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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 006044
Company: ABBVIE

Products on NDA 006044

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
DIASONE SODIUM	SULFOXONE SODIUM	165MG	TABLET, DELAYED RELEASE;ORAL	Discontinued	None	No	No

Approval Date(s) and History, Letters, Labels, Reviews for NDA 006044

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Note
03/17/1986	SUPPL-10	Labeling	Label is not available on this site.
11/27/1979	SUPPL-6	Manufacturing (CMC)-Control	Label is not available on this site.
05/24/1974	SUPPL-4		Label is not available on this site.

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