DELFLEX W/ DEXTROSE 4.25% IN PLASTIC CONTAINER Detail

Drug Name(s):
DELFLEX W/ DEXTROSE 4.25% IN PLASTIC CONTAINER

FDA Application No.:
NDA 018379

Active Ingredient(s):
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Company:
FRESENIUS MEDCL

Original Approval or Tentative Approval Date:
September 2, 1980

Products on Application NDA 018379:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE	25.7MG/100ML;2.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML	SOLUTION; INTRAPERITONEAL	Prescription	AT
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE	25.7MG/100ML;2.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML	SOLUTION; INTRAPERITONEAL	Prescription	AT
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE	25.7MG/100ML;3.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML	SOLUTION; INTRAPERITONEAL	Prescription	AT
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE	25.7MG/100ML;4.25GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML	SOLUTION; INTRAPERITONEAL	Prescription	AT

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last updated on 11-21-2008

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