URISPAS Detail

Drug Name(s):
URISPAS

FDA Application No.:
NDA 016769

Active Ingredient(s):
FLAVOXATE HYDROCHLORIDE

Company:
ORTHO MCNEIL PHARM

Original Approval or Tentative Approval Date:
July 24, 1975

Products on Application NDA 016769:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FLAVOXATE HYDROCHLORIDE	100MG	TABLET; ORAL	Prescription	AB

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last updated on 11-21-2008

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