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    Amneal Pharmaceuticals

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    ETHINYL ESTRADIOL; NORELGESTROMIN

    Brand Name : ETHINYL ESTRADIOL AND NORELGESTROMIN

    Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

    Dosage Strength : 0.035MG/24HR;0.15MG/24HR

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    Approval Date : 2021-02-25

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    Regulatory Info : Approved

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    Ethinylestradiol; Norelgestromin

    Brand Name : Euro

    Dosage Form : Transdermal Patch

    Dosage Strength : 203mcg/24hours;33.9mcg/24hours

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    Approval Date : 22/08/2002

    Application Number : 20020822000037

    Regulatory Info : Approved

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    Regulatory Info : Allowed

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    Norelgestromin; Ethinylestradiol

    Brand Name : Evra

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    Approval Date : 05/11/2003

    Application Number : 56039

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    Regulatory Info : Authorized

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    Ethinylestradiol; Norelgestromine

    Brand Name : Evra

    Dosage Form : Transdermal Patch

    Dosage Strength : 203MCG; 33.9 MCG

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    Approval Date : 2002-10-29

    Application Number : 02223001

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    Ethinylestradiol; Norelgestromine

    Brand Name : Evra

    Dosage Form : Transdermal Patch

    Dosage Strength : 203MCG; 33.9 MCG

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    Approval Date : 2003-02-04

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    Regulatory Info : Authorized

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    Ethinylestradiol; Norelgestromine

    Brand Name : Evra

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    Dosage Strength : 203MCG; 33.9 MCG

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    Approval Date : 2024-10-15

    Application Number : 02223002IP4

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    Regulatory Info : Authorized

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    Ethinylestradiol; Norelgestromine

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    Ethinylestradiol; Norelgestromine

    Brand Name : Evra

    Dosage Form : Transdermal Patch

    Dosage Strength : 203MCG; 33.9 MCG

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    Approval Date : 2017-03-14

    Application Number : 02223001IP2

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    Ethinylestradiol; Norelgestromine

    Brand Name : Evra

    Dosage Form : Transdermal Patch

    Dosage Strength : 203MCG; 33.9 MCG

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    Approval Date : 2020-04-18

    Application Number : 02223001IP4

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    Ethinylestradiol; Norelgestromine

    Brand Name : Evra

    Dosage Form : Transdermal Patch

    Dosage Strength : 203MCG; 33.9 MCG

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    Approval Date : 2016-07-07

    Application Number : 02223001IP1

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    Ethinylestradiol; Norelgestromine

    Brand Name : Evra

    Dosage Form : Transdermal Patch

    Dosage Strength : 203MCG; 33.9 MCG

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    Approval Date : 2018-10-10

    Application Number : 02223001IP3

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    Regulatory Info : Authorized

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    Ethinylestradiol; Norelgestromine

    Brand Name : Evra

    Dosage Form : Transdermal Patch

    Dosage Strength : 203MCG; 33.9 MCG

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    Approval Date : 2011-03-28

    Application Number : 02223001IP

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    Brand Name : Evra

    Dosage Form : Transdermal Patch

    Dosage Strength : 203MCG; 33.9 MCG

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    Approval Date : 2020-04-18

    Application Number : 02223002IP3

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    Ethinylestradiol; Norelgestromine

    Brand Name : Evra

    Dosage Form : Transdermal Patch

    Dosage Strength : 203MCG; 33.9 MCG

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    Approval Date : 2011-03-28

    Application Number : 02223002IP

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    Ethinylestradiol; Norelgestromine

    Brand Name : Evra

    Dosage Form : Transdermal Patch

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    Approval Date : 2018-10-10

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    Brand Name : Evra

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    Dosage Strength : 203MCG; 33.9 MCG

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    Approval Date : 2016-07-07

    Application Number : 02223002IP1

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    Johnson & Johnson Innovative Medici...

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    ETHINYL ESTRADIOL; NORELGESTROMIN

    Brand Name : ORTHO EVRA

    Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

    Dosage Strength : 0.035MG/24HR;0.15MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2001-11-20

    Application Number : 21180

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    Teva Pharmaceutical Industries

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    ETHINYL ESTRADIOL; NORELGESTROMIN

    Brand Name : ONSURA

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    Dosage Strength : 0.035MG/24HR;0.15MG/24HR

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    Approval Date : 2021-08-25

    Application Number : 213977

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    ETHINYL ESTRADIOL; NORELGESTROMIN

    Brand Name : XULANE

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    Dosage Strength : 0.035MG/24HR;0.15MG/24HR

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    Approval Date : 2014-04-16

    Application Number : 200910

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    Brand Name : ETHINYL ESTRADIOL AND NORELGESTROMIN

    Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

    Dosage Strength : 0.035MG/24HR;0.15MG/24HR

    Packaging :

    Approval Date : 2023-09-14

    Application Number : 214594

    Regulatory Info : RX

    Registration Country : USA

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