ZEBETA Detail

Drug Name(s):
ZEBETA

FDA Application No.:
NDA 019982

Active Ingredient(s):
BISOPROLOL FUMARATE

Company:
DURAMED PHARMS BARR

Original Approval or Tentative Approval Date:
June 10, 1993

Products on Application NDA 019982:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
BISOPROLOL FUMARATE	5MG	TABLET; ORAL	Prescription	AB

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last updated on 11-21-2008

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