Drug Details: BUTISOL SODIUM

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Drug Details

Drug Name:	BUTISOL SODIUM
FDA Application No:	(ANDA) 085380
Active Ingredient(s):	BUTABARBITAL SODIUM
Company:	MEDPOINTE PHARM HLC
Original Approval or Tentative Approval Date:	April 10, 1978

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
BUTISOL SODIUM	BUTABARBITAL SODIUM	30MG/5ML	ELIXIR; ORAL	Prescription	Yes	None

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On Saturday, December 6, 2014 Kathy Bunke wrote:

My father has been on Butisol sodium liquid form for over 25 years. He has been very concerned because the pharmacist says it has been discontinued. Is it still available in pill form? Is it available in liquid? Does the pill form differ in ingredients than the liquid? Any information would be greatly appreciated.