ZOLPIDEM TARTRATE Detail

Drug Name(s):
ZOLPIDEM TARTRATE

FDA Application No.:
NDA 077388

Active Ingredient(s):
ZOLPIDEM TARTRATE

Company:
CIPLA LIMITED

Original Approval or Tentative Approval Date:
October 30, 2006

Products on Application NDA 077388:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
ZOLPIDEM TARTRATE	5MG	TABLET; ORAL	Tentative approval	none

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January 2009

ZOLPIDEM TARTRATE Detail

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