ZOLPIDEM Detail

Drug Name(s):
ZOLPIDEM

FDA Application No.:
NDA 076410

Active Ingredient(s):
ZOLPIDEM TARTRATE

Company:
TEVA PHARMS

Original Approval or Tentative Approval Date:
May 25, 2005

Products on Application NDA 076410:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
ZOLPIDEM TARTRATE	10MG	TABLET; ORAL	Tentative approval	none

Recall Notices

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KRC Food Trading Inc. Recall of Fish Cake Sushi (December 23)

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January 2009

ZOLPIDEM Detail

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