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    List of All Manufacturers & Suppliers of Nafcillin Sodium Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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

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    Bora Pharmaceuticals- Making success more certain.

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

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    Axplora- The partner of choice for complex APIs.

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    Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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    Nafcillin Sodium

    ACTIVE PHARMA INGREDIENTS

    PRICE INFORMATION

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

    DIGITAL CONTENT

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

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    $ API Ref.Price (USD/KG) : 611Xls

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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

    12 12Wyeth Pharmaceuticals Inc

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    01

    Baxter Healthcare Corporation

    U.S.A
    Discovery on Target
    Not Confirmed
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    Baxter Healthcare Corporation

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
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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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    02

    Baxter Healthcare Corporation

    U.S.A
    Discovery on Target
    Not Confirmed
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    Baxter Healthcare Corporation

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
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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 2GM BASE/100ML

    Packaging :

    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
    Discovery on Target
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    Discovery on Target
    Not Confirmed
    • fda
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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

    U.S.A
    Discovery on Target
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    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
    Discovery on Target
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    NAFCILLIN SODIUM

    Brand Name : NAFCILLIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61984

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Bristol Myers Squibb

    U.S.A
    Discovery on Target
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    NAFCILLIN SODIUM

    Brand Name : NAFCILLIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61984

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    GSK

    United Kingdom
    Discovery on Target
    Not Confirmed
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    GSK

    United Kingdom
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    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    NAFCILLIN SODIUM

    Brand Name : NALLPEN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61999

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    GSK

    United Kingdom
    Discovery on Target
    Not Confirmed
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    GSK

    United Kingdom
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    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
    Discovery on Target
    Not Confirmed
    arrow

    GSK

    United Kingdom
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    Portfolio PDF

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    10

    GSK

    United Kingdom
    Discovery on Target
    Not Confirmed
    arrow

    GSK

    United Kingdom
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    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
    Luxepack
    Not Confirmed
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    Sandoz B2B

    Switzerland
    arrow
    Luxepack
    Not Confirmed
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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 : 1984-08-02

    Application Number : 62527

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Wyeth Pharmaceuticals Inc

    U.S.A
    Discovery on Target
    Not Confirmed
    arrow

    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    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
    Discovery on Target
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    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

    U.S.A
    Discovery on Target
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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

    U.S.A
    Discovery on Target
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
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    Discovery on Target
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50320

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Wyeth Pharmaceuticals Inc

    U.S.A
    Discovery on Target
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50320

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Wyeth Pharmaceuticals Inc

    U.S.A
    Discovery on Target
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50320

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Wyeth Pharmaceuticals Inc

    U.S.A
    Discovery on Target
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50320

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Wyeth Pharmaceuticals Inc

    U.S.A
    Discovery on Target
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    20

    Wyeth Pharmaceuticals Inc

    U.S.A
    Discovery on Target
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    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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