Drug Details: ANECTINE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	ANECTINE
FDA Application No:	(NDA) 008453
Active Ingredient(s):	SUCCINYLCHOLINE CHLORIDE
Company:	SANDOZ
Original Approval or Tentative Approval Date:	August 20, 1952
Chemical Type:	1 New molecular entity (NME)
Review Classification:	P Priority review drug

There are no 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
ANECTINE	SUCCINYLCHOLINE CHLORIDE	500MG/VIAL	INJECTABLE; INJECTION	Discontinued	No	None
ANECTINE	SUCCINYLCHOLINE CHLORIDE	20MG/ML	INJECTABLE; INJECTION	Prescription	Yes	AP
ANECTINE	SUCCINYLCHOLINE CHLORIDE	50MG/ML	INJECTABLE; INJECTION	Discontinued	No	None
ANECTINE	SUCCINYLCHOLINE CHLORIDE	1GM/VIAL	INJECTABLE; INJECTION	Discontinued	No	None

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