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    01 1Dr. Reddy's Laboratories

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    Dr. Reddy's Laboratories

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    CHLORDIAZEPOXIDE HYDROCHLORIDE; CLIDINIUM BROMIDE

    Brand Name : CHLORDIAZEPOXIDE HYDROCHLORIDE AND CLIDINIUM BROMIDE

    Dosage Form : CAPSULE;ORAL

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    Approval Date : 2021-05-10

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    AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

    Brand Name : CHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 12.5MG BASE;5MG

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    Approval Date : 1986-12-10

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    AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

    Brand Name : CHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE;10MG

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    Approval Date : 1986-12-10

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    Avet Pharmaceuticals

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    AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

    Brand Name : CHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 12.5MG BASE;5MG

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    Approval Date : 1988-12-16

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    Bausch & Lomb Incorporated

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    CHLORDIAZEPOXIDE HYDROCHLORIDE

    Brand Name : LIBRIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 100MG/AMP

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    Approval Date : 1982-01-01

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    Bausch & Lomb Incorporated

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    CHLORDIAZEPOXIDE HYDROCHLORIDE; CLIDINIUM BROMIDE

    Brand Name : LIBRAX

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 5MG;2.5MG

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    Approval Date : 1982-01-01

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    Bausch Health

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    CHLORDIAZEPOXIDE HYDROCHLORIDE

    Brand Name : LIBRIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-01-01

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    Bausch Health

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    CHLORDIAZEPOXIDE HYDROCHLORIDE

    Brand Name : LIBRIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-01-01

    Application Number : 12249

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    09

    Bausch Health

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    CHLORDIAZEPOXIDE HYDROCHLORIDE

    Brand Name : LIBRIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-01-01

    Application Number : 12249

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    Bausch Health

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    Bausch Health

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    Regulatory Info : DISCN

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    CHLORDIAZEPOXIDE

    Brand Name : LIBRELEASE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 30MG

    Packaging :

    Approval Date : 1983-09-12

    Application Number : 17813

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    11

    Chartwell Pharmaceuticals llc

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    Chartwell Pharmaceuticals llc

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    AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

    Brand Name : LIMBITROL

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 12.5MG BASE;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 16949

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    Registration Country : USA

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    12

    Chartwell Pharmaceuticals llc

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    Chartwell Pharmaceuticals llc

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    AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

    Brand Name : LIMBITROL DS

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 16949

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    13

    F. Hoffmann-La Roche

    Switzerland
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    F. Hoffmann-La Roche

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    Regulatory Info : DISCN

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    CHLORDIAZEPOXIDE; ESTROGENS, ESTERIFIED

    Brand Name : MENRIUM 5-2

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG;0.2MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 14740

    Regulatory Info : DISCN

    Registration Country : USA

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    F. Hoffmann-La Roche

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    CHLORDIAZEPOXIDE; ESTROGENS, ESTERIFIED

    Brand Name : MENRIUM 5-4

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG;0.4MG

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    Approval Date : 1982-01-01

    Application Number : 14740

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    Registration Country : USA

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    F. Hoffmann-La Roche

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    CHLORDIAZEPOXIDE; ESTROGENS, ESTERIFIED

    Brand Name : MENRIUM 10-4

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG;0.4MG

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    Approval Date : 1982-01-01

    Application Number : 14740

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    USL PHARMA

    United Kingdom
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    USL PHARMA

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    AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

    Brand Name : CHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 12.5MG BASE;5MG

    Packaging :

    Approval Date : 1988-01-12

    Application Number : 70477

    Regulatory Info : DISCN

    Registration Country : USA

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    USL PHARMA

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    USL PHARMA

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    AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

    Brand Name : CHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE;10MG

    Packaging :

    Approval Date : 1988-01-12

    Application Number : 70478

    Regulatory Info : DISCN

    Registration Country : USA

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    Viatris

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    Viatris

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    Regulatory Info :

    Registration Country : USA

    AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

    Brand Name : CHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE

    Dosage Form : TABLET; ORAL

    Dosage Strength : EQ 12.5MG BASE;5MG

    Packaging :

    Approval Date :

    Application Number : 71296

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    Registration Country : USA

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    Viatris

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    Viatris

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    Regulatory Info : RX

    Registration Country : USA

    AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

    Brand Name : CHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE;10MG

    Packaging :

    Approval Date : 1986-12-10

    Application Number : 71297

    Regulatory Info : RX

    Registration Country : USA

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    Viatris

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    Viatris

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    Regulatory Info : RX

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    AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

    Brand Name : CHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 12.5MG BASE;5MG

    Packaging :

    Approval Date : 1986-12-10

    Application Number : 71297

    Regulatory Info : RX

    Registration Country : USA

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