NABUMETONE Detail

Drug Name(s):
NABUMETONE

FDA Application No.:
NDA 075189

Active Ingredient(s):
NABUMETONE

Company:
TEVA

Original Approval or Tentative Approval Date:
May 25, 2000

Products on Application NDA 075189:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NABUMETONE	500MG	TABLET; ORAL	Prescription	AB

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last updated on 12-01-2008

NABUMETONE Detail

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