Drug Details: RESERPINE AND HYDROFLUMETHIAZIDE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	RESERPINE AND HYDROFLUMETHIAZIDE
FDA Application No:	(ANDA) 088907
Active Ingredient(s):	HYDROFLUMETHIAZIDE; RESERPINE
Company:	PAR PHARM
Original Approval or Tentative Approval Date:	September 20, 1985

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
RESERPINE AND HYDROFLUMETHIAZIDE	HYDROFLUMETHIAZIDE; RESERPINE	50MG; 0.125MG	TABLET; ORAL	Discontinued	No	None

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