FENOPROFEN CALCIUM Detail

Drug Name(s):
FENOPROFEN CALCIUM

FDA Application No.:
NDA 071738

Active Ingredient(s):
FENOPROFEN CALCIUM

Company:
QUANTUM PHARMICS

Original Approval or Tentative Approval Date:
August 25, 1988

Products on Application NDA 071738:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FENOPROFEN CALCIUM	EQ 300MG BASE	CAPSULE; ORAL	Discontinued	none

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last updated on 12-01-2008