NALIDIXIC ACID Detail

Drug Name(s):
NALIDIXIC ACID

FDA Application No.:
NDA 071919

Active Ingredient(s):
NALIDIXIC ACID

Company:
WATSON LABS

Original Approval or Tentative Approval Date:
June 28, 1990

Products on Application NDA 071919:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NALIDIXIC ACID	1GM	TABLET; ORAL	Prescription	AB

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last updated on 12-01-2008

NALIDIXIC ACID Detail

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