Drug Details: ESTRADIOL

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	ESTRADIOL
FDA Application No:	(NDA) 020538
Active Ingredient(s):	ESTRADIOL
Company:	NOVARTIS
Original Approval or Tentative Approval Date:	July 31, 1996
Chemical Type:	5 New manufacturer
Review Classification:	S Standard review drug

Therapeutic Equivalents	Label Information
Approval History, Letters, Reviews and Related Documents

You can see the products in the same application. The table can be sorted by clicking the header columns.

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
ESTRADIOL	ESTRADIOL	0.0375MG/24HR	Film, Extended Release; Transdermal	Discontinued	No	None
ESTRADIOL	ESTRADIOL	0.075MG/24HR	Film, Extended Release; Transdermal	Discontinued	No	None
ESTRADIOL	ESTRADIOL	0.05MG/24HR	Film, Extended Release; Transdermal	Discontinued	No	None
ESTRADIOL	ESTRADIOL	0.1MG/24HR	Film, Extended Release; Transdermal	Discontinued	No	None
VIVELLE-DOT	ESTRADIOL	0.0375MG/24HR	FILM, EXTENDED RELEASE; TRANSDERMAL	Prescription	No	BX
VIVELLE-DOT	ESTRADIOL	0.05MG/24HR	FILM, EXTENDED RELEASE; TRANSDERMAL	Prescription	No	AB1
VIVELLE-DOT	ESTRADIOL	0.075MG/24HR	FILM, EXTENDED RELEASE; TRANSDERMAL	Prescription	No	BX
VIVELLE-DOT	ESTRADIOL	0.1MG/24HR	FILM, EXTENDED RELEASE; TRANSDERMAL	Prescription	Yes	AB1
VIVELLE-DOT	ESTRADIOL	0.025MG/24HR	FILM, EXTENDED RELEASE; TRANSDERMAL	Prescription	No	BX

Comments for ESTRADIOL

Name: *

Email: *

Text:
(HTML OK)

Enter the code from the picture: *
(click here to load another image)

There are no comments.