OMNICEF Detail

Drug Name(s):
OMNICEF

FDA Application No.:
NDA 050739

Active Ingredient(s):
CEFDINIR

Company:
ABBOTT

Original Approval or Tentative Approval Date:
December 3, 1997

Products on Application NDA 050739:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CEFDINIR	300MG	CAPSULE; ORAL	Prescription	AB

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last updated on 01-08-2009

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