Drug Details: CLIMARA

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	CLIMARA
FDA Application No:	(NDA) 020375
Active Ingredient(s):	ESTRADIOL
Company:	BAYER HLTHC
Original Approval or Tentative Approval Date:	December 22, 1994
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
CLIMARA	ESTRADIOL	0.05MG/24HR	FILM, EXTENDED RELEASE; TRANSDERMAL	Prescription	No	AB2
CLIMARA	ESTRADIOL	0.1MG/24HR	FILM, EXTENDED RELEASE; TRANSDERMAL	Prescription	Yes	AB2
CLIMARA	ESTRADIOL	0.075MG/24HR	FILM, EXTENDED RELEASE; TRANSDERMAL	Prescription	No	AB2
CLIMARA	ESTRADIOL	0.025MG/24HR	FILM, EXTENDED RELEASE; TRANSDERMAL	Prescription	No	AB2
CLIMARA	ESTRADIOL	0.0375MG/24HR	FILM, EXTENDED RELEASE; TRANSDERMAL	Prescription	No	AB
CLIMARA	ESTRADIOL	0.06MG/24HR	FILM, EXTENDED RELEASE; TRANSDERMAL	Prescription	No	AB

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