MAXALT Detail

FDA Consumer Information Sheet:

Consumer Information Sheet

Drug Name(s):
MAXALT

FDA Application No.:
NDA 020864

Active Ingredient(s):
RIZATRIPTAN BENZOATE

Company:
MERCK

Original Approval or Tentative Approval Date:
June 28, 1998

Products on Application NDA 020864:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
RIZATRIPTAN BENZOATE	EQ 10MG BASE	TABLET; ORAL	Prescription	none

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last updated on 11-21-2008

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