UCEPHAN Detail

Drug Name(s):
UCEPHAN

FDA Application No.:
NDA 019530

Active Ingredient(s):
SODIUM BENZOATE; SODIUM PHENYLACETATE

Company:
B BRAUN

Original Approval or Tentative Approval Date:
December 22, 1987

Products on Application NDA 019530:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
SODIUM BENZOATE; SODIUM PHENYLACETATE	100MG/ML;100MG/ML	SOLUTION; ORAL	Discontinued	none

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last updated on 11-21-2008

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