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    Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.

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    Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.

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    01 1Dr. Reddy's Laboratories

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    Dr. Reddy's Laboratories

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    Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    CHLORDIAZEPOXIDE HYDROCHLORIDE; CLIDINIUM BROMIDE

    Brand Name : CHLORDIAZEPOXIDE HYDROCHLORIDE AND CLIDINIUM BROMIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 5MG;2.5MG

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    Approval Date : 2021-05-10

    Application Number : 214698

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    02

    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

    Application Number : 72052

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    03

    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

    Application Number : 12301

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    04

    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

    Application Number : 12750

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    05

    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

    Application Number : 12249

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    Registration Country : USA

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    06

    Bausch Health

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    Regulatory Info : DISCN

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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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    07

    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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    Registration Country : USA

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    08

    Bausch Health

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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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    Registration Country : USA

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    09

    Chartwell Pharmaceuticals llc

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    Regulatory Info : DISCN

    Registration Country : USA

    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

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Chartwell Pharmaceuticals llc

    U.S.A
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    Chartwell Pharmaceuticals llc

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    Regulatory Info : DISCN

    Registration Country : USA

    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

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    F. Hoffmann-La Roche

    Switzerland
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    Switzerland
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    12

    F. Hoffmann-La Roche

    Switzerland
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    F. Hoffmann-La Roche

    Switzerland
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    SCOPE Summit
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    Regulatory Info : DISCN

    Registration Country : USA

    CHLORDIAZEPOXIDE; ESTROGENS, ESTERIFIED

    Brand Name : MENRIUM 5-4

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG;0.4MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 14740

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    F. Hoffmann-La Roche

    Switzerland
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    F. Hoffmann-La Roche

    Switzerland
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    Regulatory Info : DISCN

    Registration Country : USA

    CHLORDIAZEPOXIDE; ESTROGENS, ESTERIFIED

    Brand Name : MENRIUM 10-4

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG;0.4MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 14740

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Tulex Pharmaceutical

    U.S.A
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    Tulex Pharmaceutical

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    Regulatory Info : DISCN

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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 : 70765

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Tulex Pharmaceutical

    U.S.A
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    Tulex Pharmaceutical

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    Regulatory Info : DISCN

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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 : 1986-12-10

    Application Number : 70766

    Regulatory Info : DISCN

    Registration Country : USA

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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

    United Kingdom
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    USL PHARMA

    United Kingdom
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    Regulatory Info : DISCN

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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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    18

    Viatris

    U.S.A
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    Viatris

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    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

    Regulatory Info :

    Registration Country : USA

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    19

    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

    U.S.A
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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 12.5MG BASE;5MG

    Packaging :

    Approval Date : 1986-12-10

    Application Number : 71297

    Regulatory Info : RX

    Registration Country : USA

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.