NATEGLINIDE Detail

Drug Name(s):
NATEGLINIDE

FDA Application No.:
NDA 077463

Active Ingredient(s):
NATEGLINIDE

Company:
PAR PHARM

Original Approval or Tentative Approval Date:
August 9, 2006

Products on Application NDA 077463:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NATEGLINIDE	60MG	TABLET; ORAL	Tentative approval	none

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last updated on 12-05-2008

NATEGLINIDE Detail

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