Drug Details: FEMCON FE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	FEMCON FE
FDA Application No:	(NDA) 021490
Active Ingredient(s):	ETHINYL ESTRADIOL; NORETHINDRONE
Company:	WARNER CHILCOTT
Original Approval or Tentative Approval Date:	November 14, 2003
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug

There are no Therapeutic Equivalents	Label Information
Approval History, Letters, Reviews and Related Documents

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Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
FEMCON FE	ETHINYL ESTRADIOL; NORETHINDRONE	0.035MG; 0.4MG	TABLET, CHEWABLE; ORAL-28	Prescription	Yes	None

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