GLIPIZIDE Detail

Drug Name(s):
GLIPIZIDE

FDA Application No.:
NDA 074223

Active Ingredient(s):
GLIPIZIDE

Company:
WATSON LABS

Original Approval or Tentative Approval Date:
February 26, 1995

Products on Application NDA 074223:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
GLIPIZIDE	5MG	TABLET; ORAL	Prescription	AB

Recall Notices

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January 2009

GLIPIZIDE Detail

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