Drug Details: QUINIDINE SULFATE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	QUINIDINE SULFATE
FDA Application No:	(ANDA) 083743
Active Ingredient(s):	QUINIDINE SULFATE
Company:	LANNETT
Original Approval or Tentative Approval Date:	January 14, 1977

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
QUINIDINE SULFATE	QUINIDINE SULFATE	200MG	TABLET; ORAL	Discontinued	No	None

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