FENOPROFEN CALCIUM Detail

Drug Name(s):
FENOPROFEN CALCIUM

FDA Application No.:
NDA 072602

Active Ingredient(s):
FENOPROFEN CALCIUM

Company:
WATSON LABS

Original Approval or Tentative Approval Date:
October 10, 1988

Products on Application NDA 072602:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FENOPROFEN CALCIUM	EQ 600MG BASE	TABLET; ORAL	Prescription	AB

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last updated on 12-01-2008