NABUMETONE Detail

Drug Name(s):
NABUMETONE

FDA Application No.:
NDA 075280

Active Ingredient(s):
NABUMETONE

Company:
SANDOZ

Original Approval or Tentative Approval Date:
February 24, 2002

Products on Application NDA 075280:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NABUMETONE	750MG	TABLET; ORAL	Prescription	AB

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last updated on 11-19-2008

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