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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.

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

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    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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

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    Nafcillin Sodium

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    01 6Actavis Inc

    02 4Antibiotice SA

    03 3Aurobindo Pharma Limited

    04 2Baxter Healthcare Corporation

    05 4Bristol Myers Squibb

    06 3Fresenius Medical Care

    07 6GSK

    08 3Istituto Biochimico Italiano Giovanni Lorenzini SpA

    09 2STERISCIENCE SPECLTS

    10 3Sagent Pharmaceuticals

    11 6Sandoz B2B

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    Baxter Healthcare Corporation

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    NAFCILLIN SODIUM

    Brand Name : NALLPEN IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20MG BASE/ML

    Packaging :

    Approval Date : 1989-10-31

    Application Number : 50655

    Regulatory Info : RX

    Registration Country : USA

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    Baxter Healthcare Corporation

    U.S.A
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    Regulatory Info : RX

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    NAFCILLIN SODIUM

    Brand Name : NALLPEN IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/100ML

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    Approval Date : 1989-10-31

    Application Number : 50655

    Regulatory Info : RX

    Registration Country : USA

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    03

    Bristol Myers Squibb

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    NAFCILLIN SODIUM

    Brand Name : NAFCILLIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61984

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Bristol Myers Squibb

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    Regulatory Info : DISCN

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    NAFCILLIN SODIUM

    Brand Name : NAFCILLIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61984

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Bristol Myers Squibb

    U.S.A
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    Regulatory Info : DISCN

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    NAFCILLIN SODIUM

    Brand Name : NAFCILLIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

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    Approval Date : 1982-01-01

    Application Number : 61984

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Bristol Myers Squibb

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    Regulatory Info : DISCN

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    NAFCILLIN SODIUM

    Brand Name : NAFCILLIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4GM BASE/VIAL

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    Approval Date : 1982-01-01

    Application Number : 61984

    Regulatory Info : DISCN

    Registration Country : USA

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    GSK

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    Regulatory Info : DISCN

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    NAFCILLIN SODIUM

    Brand Name : NALLPEN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

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    Approval Date : 1982-01-01

    Application Number : 61999

    Regulatory Info : DISCN

    Registration Country : USA

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    GSK

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    Regulatory Info : DISCN

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    NAFCILLIN SODIUM

    Brand Name : NALLPEN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61999

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    GSK

    United Kingdom
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    GSK

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    Regulatory Info : DISCN

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    NAFCILLIN SODIUM

    Brand Name : NALLPEN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61999

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    GSK

    United Kingdom
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    GSK

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    Regulatory Info : DISCN

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    NAFCILLIN SODIUM

    Brand Name : NALLPEN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61999

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Sandoz B2B

    Switzerland
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    Switzerland
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    Regulatory Info : DISCN

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    NAFCILLIN SODIUM

    Brand Name : NAFCILLIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1984-08-02

    Application Number : 62527

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Wyeth Pharmaceuticals Inc

    U.S.A
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    Regulatory Info : DISCN

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    NAFCILLIN SODIUM

    Brand Name : UNIPEN

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 250MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50111

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Wyeth Pharmaceuticals Inc

    U.S.A
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    NAFCILLIN SODIUM

    Brand Name : UNIPEN

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : EQ 250MG BASE/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50199

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Wyeth Pharmaceuticals Inc

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    NAFCILLIN SODIUM

    Brand Name : UNIPEN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50320

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Wyeth Pharmaceuticals Inc

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    Regulatory Info : DISCN

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    NAFCILLIN SODIUM

    Brand Name : UNIPEN IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/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 : 50320

    Regulatory Info : DISCN

    Registration Country : USA

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    Wyeth Pharmaceuticals Inc

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    Regulatory Info : DISCN

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    NAFCILLIN SODIUM

    Brand Name : UNIPEN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/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 : 50320

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Wyeth Pharmaceuticals Inc

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    NAFCILLIN SODIUM

    Brand Name : UNIPEN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4GM BASE/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 : 50320

    Regulatory Info : DISCN

    Registration Country : USA

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    Wyeth Pharmaceuticals Inc

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    NAFCILLIN SODIUM

    Brand Name : UNIPEN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10GM BASE/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 : 50320

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    Registration Country : USA

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    Wyeth Pharmaceuticals Inc

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    Regulatory Info : DISCN

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    NAFCILLIN SODIUM

    Brand Name : UNIPEN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50320

    Regulatory Info : DISCN

    Registration Country : USA

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    Wyeth Pharmaceuticals Inc

    U.S.A
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    Regulatory Info : DISCN

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    NAFCILLIN SODIUM

    Brand Name : UNIPEN

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 500MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50462

    Regulatory Info : DISCN

    Registration Country : USA

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