Drug Details: AMINOSYN 3.5%

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	AMINOSYN 3.5%
FDA Application No:	(NDA) 017789
Active Ingredient(s):	AMINO ACIDS
Company:	HOSPIRA
Original Approval or Tentative Approval Date:	May 14, 1976
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug

Therapeutic Equivalents	Labels are not available
Approval History, Letters, Reviews and Related Documents

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Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
AMINOSYN 3.5%	AMINO ACIDS	3.5% (3.5GM/100ML)	INJECTABLE; INJECTION	Prescription	No	None
AMINOSYN 3.5% M	AMINO ACIDS; MAGNESIUM ACETATE; POTASSIUM ACETATE; SODIUM CHLORIDE	3.5%; 21MG/100ML; 128MG/100ML; 234MG/100ML	INJECTABLE; INJECTION	Discontinued	No	None
AMINOSYN 3.5% M	AMINO ACIDS; MAGNESIUM ACETATE; PHOSPHORIC ACID; POTASSIUM ACETATE; SODIUM CHLORIDE	3.5%; 21MG/100ML; 40MG/100ML; 128MG/100ML; 234MG/100ML	INJECTABLE; INJECTION	Prescription	No	None
AMINOSYN 7% W/ ELECTROLYTES	AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE	7%; 102MG/100ML; 522MG/100ML; 410MG/100ML	INJECTABLE; INJECTION	Prescription	No	None

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