ULTRACEF Detail

Drug Name(s):
ULTRACEF

FDA Application No.:
NDA 062408

Active Ingredient(s):
CEFADROXIL/CEFADROXIL HEMIHYDRATE

Company:
BRISTOL

Products on Application NDA 062408:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CEFADROXIL/CEFADROXIL HEMIHYDRATE	EQ 1GM BASE	TABLET; ORAL	Discontinued	none

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last updated on 12-01-2008

ULTRACEF Detail

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