OMNICEF Detail

Drug Name(s):
OMNICEF

FDA Application No.:
NDA 050749

Active Ingredient(s):
CEFDINIR

Company:
ABBOTT

Original Approval or Tentative Approval Date:
April 21, 1998

Products on Application NDA 050749:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CEFDINIR	250MG/5ML	FOR SUSPENSION; ORAL	Prescription	none

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January 2009

OMNICEF Detail

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