GLIPIZIDE Detail

Drug Name(s):
GLIPIZIDE

FDA Application No.:
NDA 074387

Active Ingredient(s):
GLIPIZIDE

Company:
TEVA

Original Approval or Tentative Approval Date:
November 18, 1999

Products on Application NDA 074387:

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

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last updated on 01-07-2009

GLIPIZIDE Detail

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