ZMAX Detail

Drug Name(s):
ZMAX

FDA Application No.:
NDA 050797

Active Ingredient(s):
AZITHROMYCIN

Company:
PFIZER GLOBAL

Original Approval or Tentative Approval Date:
June 9, 2005

Products on Application NDA 050797:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
AZITHROMYCIN	EQ 2GM BASE/BOT	FOR SUSPENSION, EXTENDED RELEASE; ORAL	Prescription	none

Recall Notices

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January 2009

ZMAX Detail

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