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    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    Lupin Manufacturing Solutions – delivering high-quality APIs & end-to-end CDMO services for faster, cost-effective drug development.

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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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    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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    01 1AbbVie Inc

    02 1Biophore India Pharmaceuticals Pvt Ltd

    03 2Dr. Reddy's Laboratories

    04 1ABRAXIS PHARM

    05 1Abbott Laboratories

    06 1Adcock Ingram

    07 1Amneal Pharmaceuticals

    08 1Amphastar Pharmaceuticals

    09 1Aurobindo Pharma Limited

    10 1Avet Pharmaceuticals

    11 1Bausch Health

    12 1Baxter Healthcare Corporation

    13 2Biological E

    14 1Caplin Point Laboratories Limited

    15 1Chartwell Pharmaceuticals llc

    16 1Cipla

    17 1EJ Busuttil Ltd

    18 1Epic Pharma. LLC.

    19 1Etico Lifesciences

    20 3Exela Pharma Sciences, LLC.

    21 1F. Hoffmann-La Roche

    22 4Farbe Firma

    23 1Genchain Biotech

    24 1Hainan Poly Pharm

    25 1Hospira, Inc.

    26 1JAMP PHARMA

    27 1MARCAN PHARMACEUTICALS INC

    28 1Micro Labs Limited

    29 1Nexus Pharmaceuticals

    30 1ORIFARM GROUP AS

    31 1Oresund Pharma Aps

    32 1Ospedalia Ag

    33 1PHARMOBEDIENT

    34 1Pfizer Inc

    35 1STERIMAX INC

    36 1Sagent Pharmaceuticals

    37 4Slate Run Pharmaceuticals

    38 1Solfran Laboratories

    39 1Somerset Pharmaceuticals Inc

    40 1Sun Pharmaceutical Industries Limited

    41 1Teva Pharmaceutical Industries

    42 1Urquima S.A. Grupo Uriach

    43 2Viatris

    44 1Xiromed

    45 1Øresund Pharma ApS

    46 1Øresund Pharma Aps

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    01

    AbbVie Inc

    U.S.A
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    Regulatory Info : DISCN

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    SODIUM NITROPRUSSIDE

    Brand Name : NITROPRESS

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/VIAL **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 : 18450

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Biophore India Pharmaceuticals Pvt ...

    India
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    Virtual BoothBiophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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    Sodium Nitroprusside

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    Dosage Form : Injection

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    Biophore

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    03

    Dr. Reddy's Laboratories

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

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    Regulatory Info : RX

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    SODIUM NITROPRUSSIDE

    Brand Name : SODIUM NITROPRUSSIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML

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    Approval Date : 2019-04-10

    Application Number : 210114

    Regulatory Info : RX

    Registration Country : USA

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    04

    Dr. Reddy's Laboratories

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

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    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

    SODIUM NITROPRUSSIDE

    Brand Name : SODIUM NITROPRUSSIDE FOR INJECTION

    Dosage Form : SOLUTION

    Dosage Strength : 25MG/ML

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    Application Number : 2507404

    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

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    05

    Abbott Laboratories

    U.S.A
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    SODIUM NITROPRUSSIDE

    Brand Name : NITROPRESS

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/VIAL

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    Approval Date : 1987-11-16

    Application Number : 71555

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    Registration Country : USA

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    06

    ABRAXIS PHARM

    U.S.A
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    ABRAXIS PHARM

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    SODIUM NITROPRUSSIDE

    Brand Name : SODIUM NITROPRUSSIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/VIAL

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    Approval Date : 1985-01-17

    Application Number : 70031

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Amneal Pharmaceuticals

    U.S.A
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    Amneal Pharmaceuticals

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    Regulatory Info : RX

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    SODIUM NITROPRUSSIDE

    Brand Name : SODIUM NITROPRUSSIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML

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    Approval Date : 2017-11-07

    Application Number : 209493

    Regulatory Info : RX

    Registration Country : USA

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    08

    Avet Pharmaceuticals

    U.S.A
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    SODIUM NITROPRUSSIDE

    Brand Name : SODIUM NITROPRUSSIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML

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    Approval Date : 2022-11-08

    Application Number : 208923

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Bausch Health

    Canada
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    Bausch Health

    Canada
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    Regulatory Info : DISCN

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    SODIUM NITROPRUSSIDE

    Brand Name : NITROPRESS

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML

    Packaging :

    Approval Date : 1988-08-01

    Application Number : 71961

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Baxter Healthcare Corporation

    U.S.A
    Health 2.0 Conference
    Not Confirmed
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    Baxter Healthcare Corporation

    U.S.A
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    Health 2.0 Conference
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    Regulatory Info : DISCN

    Registration Country : USA

    SODIUM NITROPRUSSIDE

    Brand Name : SODIUM NITROPRUSSIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-07-28

    Application Number : 18581

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Epic Pharma. LLC.

    U.S.A
    Health 2.0 Conference
    Not Confirmed
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    Epic Pharma. LLC.

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    SODIUM NITROPRUSSIDE

    Brand Name : SODIUM NITROPRUSSIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML

    Packaging :

    Approval Date : 2017-05-04

    Application Number : 208635

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Exela Pharma Sciences, LLC.

    U.S.A
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    Not Confirmed
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    Exela Pharma Sciences, LLC.

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM NITROPRUSSIDE

    Brand Name : NIPRIDE RTU IN SODIUM CHLORIDE 0.9%

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 50MG/100ML (0.5MG/ML)

    Packaging :

    Approval Date : 2017-03-08

    Application Number : 209387

    Regulatory Info : RX

    Registration Country : USA

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    13

    Exela Pharma Sciences, LLC.

    U.S.A
    Health 2.0 Conference
    Not Confirmed
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    Exela Pharma Sciences, LLC.

    U.S.A
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    Regulatory Info : DISCN

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    SODIUM NITROPRUSSIDE

    Brand Name : NIPRIDE RTU IN SODIUM CHLORIDE 0.9%

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 10MG/50ML (0.2MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2017-12-07

    Application Number : 209387

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Exela Pharma Sciences, LLC.

    U.S.A
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    Exela Pharma Sciences, LLC.

    U.S.A
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    Regulatory Info : RX

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    SODIUM NITROPRUSSIDE

    Brand Name : NIPRIDE RTU IN SODIUM CHLORIDE 0.9%

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 20MG/100ML (0.2MG/ML)

    Packaging :

    Approval Date : 2018-07-13

    Application Number : 209387

    Regulatory Info : RX

    Registration Country : USA

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    15

    F. Hoffmann-La Roche

    Switzerland
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    F. Hoffmann-La Roche

    Switzerland
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    Regulatory Info : DISCN

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    SODIUM NITROPRUSSIDE

    Brand Name : NIPRIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 17546

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Hospira, Inc.

    U.S.A
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    Hospira, Inc.

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    Regulatory Info : DISCN

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    SODIUM NITROPRUSSIDE

    Brand Name : NITROPRESS

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/VIAL

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    Approval Date : 1986-06-09

    Application Number : 70566

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Micro Labs Limited

    India
    Health 2.0 Conference
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    Micro Labs Limited

    India
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    SODIUM NITROPRUSSIDE

    Brand Name : SODIUM NITROPRUSSIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML

    Packaging :

    Approval Date : 2017-12-08

    Application Number : 209352

    Regulatory Info : RX

    Registration Country : USA

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    18

    Nexus Pharmaceuticals

    U.S.A
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    Regulatory Info : RX

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    SODIUM NITROPRUSSIDE

    Brand Name : SODIUM NITROPRUSSIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML

    Packaging :

    Approval Date : 2017-05-25

    Application Number : 207499

    Regulatory Info : RX

    Registration Country : USA

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    19

    Sagent Pharmaceuticals

    U.S.A
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    Sagent Pharmaceuticals

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    SODIUM NITROPRUSSIDE

    Brand Name : SODIUM NITROPRUSSIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML

    Packaging :

    Approval Date : 2016-12-08

    Application Number : 207426

    Regulatory Info : RX

    Registration Country : USA

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    20

    Teva Pharmaceutical Industries

    Israel
    Health 2.0 Conference
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    Teva Pharmaceutical Industries

    Israel
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    Regulatory Info : DISCN

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    SODIUM NITROPRUSSIDE

    Brand Name : SODIUM NITROPRUSSIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML

    Packaging :

    Approval Date : 1992-03-30

    Application Number : 73465

    Regulatory Info : DISCN

    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.