NALIDIXIC ACID Detail

Drug Name(s):
NALIDIXIC ACID

FDA Application No.:
NDA 071936

Active Ingredient(s):
NALIDIXIC ACID

Company:
WATSON LABS

Original Approval or Tentative Approval Date:
June 27, 1988

Products on Application NDA 071936:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NALIDIXIC ACID	250MG	TABLET; ORAL	Prescription	AB

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last updated on 12-01-2008

NALIDIXIC ACID Detail

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