FENOLDOPAM MESYLATE Detail

Drug Name(s):
FENOLDOPAM MESYLATE

FDA Application No.:
NDA 076582

Active Ingredient(s):
FENOLDOPAM MESYLATE

Company:
BEDFORD LABS

Original Approval or Tentative Approval Date:
October 11, 2004

Products on Application NDA 076582:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FENOLDOPAM MESYLATE	EQ 10MG BASE/ML	INJECTABLE; INJECTION	Prescription	AP

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last updated on 12-05-2008