RENOQUID Detail

Drug Name(s):
RENOQUID

FDA Application No.:
NDA 017569

Active Ingredient(s):
SULFACYTINE

Company:
GLENWOOD

Original Approval or Tentative Approval Date:
September 11, 1975

Products on Application NDA 017569:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
SULFACYTINE	250MG	TABLET; ORAL	Discontinued	none

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last updated on 11-21-2008

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