RAPTIVA Detail

FDA Consumer Information Sheet:

Consumer Information Sheet

Drug Name(s):
RAPTIVA

FDA Application No.:
BLA 125075

Active Ingredient(s):
EFALIZUMAB

Company:
GENENTECH

Original Approval or Tentative Approval Date:
October 26, 2003

Products on Application BLA 125075:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
EFALIZUMAB	125MG/VIAL	VIAL; SUBCUTANEOUS	Prescription	none

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last updated on 11-21-2008

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