NADOLOL Detail

Drug Name(s):
NADOLOL

FDA Application No.:
NDA 074172

Active Ingredient(s):
NADOLOL

Company:
MYLAN

Original Approval or Tentative Approval Date:
February 4, 1998

Products on Application NDA 074172:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NADOLOL	20MG	TABLET; ORAL	Prescription	AB
NADOLOL	80MG	TABLET; ORAL	Prescription	AB

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last updated on 12-01-2008

NADOLOL Detail

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