ZOLPIDEM Detail

Drug Name(s):
ZOLPIDEM

FDA Application No.:
NDA 077359

Active Ingredient(s):
ZOLPIDEM TARTRATE

Company:
CARACO

Original Approval or Tentative Approval Date:
August 18, 2005

Products on Application NDA 077359:

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

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last updated on 12-05-2008

ZOLPIDEM Detail

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