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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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    Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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

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    Gentec Pharmaceutical Group is focused on manufacturing & developing APIs/HPAPIs, Advanced Intermediates & Fine Chemicals.

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    Nafcillin Sodium

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

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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

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    Baxter Healthcare Corporation

    U.S.A
    Immuno-Oncology 360
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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

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    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
    Immuno-Oncology 360
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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

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    03

    Bristol Myers Squibb

    U.S.A
    Immuno-Oncology 360
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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

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    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
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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

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    Approval Date : 1982-01-01

    Application Number : 61984

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    Registration Country : USA

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    05

    Bristol Myers Squibb

    U.S.A
    Immuno-Oncology 360
    Not Confirmed
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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

    U.S.A
    Immuno-Oncology 360
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    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 4GM BASE/VIAL

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    Approval Date : 1982-01-01

    Application Number : 61984

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    Registration Country : USA

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    07

    GSK

    United Kingdom
    Immuno-Oncology 360
    Not Confirmed
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    GSK

    United Kingdom
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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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    08

    GSK

    United Kingdom
    Immuno-Oncology 360
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    GSK

    United Kingdom
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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
    Immuno-Oncology 360
    Not Confirmed
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    GSK

    United Kingdom
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    Immuno-Oncology 360
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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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    10

    GSK

    United Kingdom
    Immuno-Oncology 360
    Not Confirmed
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    GSK

    United Kingdom
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    Immuno-Oncology 360
    Not Confirmed
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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

    GSK

    United Kingdom
    Immuno-Oncology 360
    Not Confirmed
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    GSK

    United Kingdom
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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 : 1986-12-19

    Application Number : 62755

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    GSK

    United Kingdom
    Immuno-Oncology 360
    Not Confirmed
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    GSK

    United Kingdom
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    Immuno-Oncology 360
    Not Confirmed
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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 : 1986-12-19

    Application Number : 62755

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Sandoz B2B

    Switzerland
    Cancer Research
    Not Confirmed
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    Sandoz B2B

    Switzerland
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    Cancer Research
    Not Confirmed
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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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    14

    Sandoz B2B

    Switzerland
    Immuno-Oncology 360
    Not Confirmed
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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 1GM BASE/VIAL

    Packaging :

    Approval Date : 1984-08-02

    Application Number : 62527

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Sandoz B2B

    Switzerland
    Immuno-Oncology 360
    Not Confirmed
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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

    Packaging :

    Approval Date : 1984-08-02

    Application Number : 62527

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Sandoz B2B

    Switzerland
    Immuno-Oncology 360
    Not Confirmed
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    Switzerland
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    Immuno-Oncology 360
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    Regulatory Info : DISCN

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    NAFCILLIN SODIUM

    Brand Name : NAFCILLIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10GM BASE/VIAL

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    Approval Date : 1984-08-02

    Application Number : 62527

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Sandoz B2B

    Switzerland
    Immuno-Oncology 360
    Not Confirmed
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    Switzerland
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    Immuno-Oncology 360
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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 : 1986-12-23

    Application Number : 62732

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Sandoz B2B

    Switzerland
    Immuno-Oncology 360
    Not Confirmed
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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 2GM BASE/VIAL

    Packaging :

    Approval Date : 1986-12-23

    Application Number : 62732

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Wyeth Pharmaceuticals Inc

    U.S.A
    Immuno-Oncology 360
    Not Confirmed
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    U.S.A
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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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    20

    Wyeth Pharmaceuticals Inc

    U.S.A
    Immuno-Oncology 360
    Not Confirmed
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    U.S.A
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    Regulatory Info : DISCN

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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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    21

    Wyeth Pharmaceuticals Inc

    U.S.A
    Immuno-Oncology 360
    Not Confirmed
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    U.S.A
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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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    22

    Wyeth Pharmaceuticals Inc

    U.S.A
    Immuno-Oncology 360
    Not Confirmed
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    U.S.A
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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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    Wyeth Pharmaceuticals Inc

    U.S.A
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    Not Confirmed
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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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50320

    Regulatory Info : DISCN

    Registration Country : USA

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    24

    Wyeth Pharmaceuticals Inc

    U.S.A
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    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
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    Immuno-Oncology 360
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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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    25

    Wyeth Pharmaceuticals Inc

    U.S.A
    Immuno-Oncology 360
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
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    Immuno-Oncology 360
    Not Confirmed
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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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    26

    Wyeth Pharmaceuticals Inc

    U.S.A
    Immuno-Oncology 360
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
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    Immuno-Oncology 360
    Not Confirmed
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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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    27

    Wyeth Pharmaceuticals Inc

    U.S.A
    Immuno-Oncology 360
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
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    Immuno-Oncology 360
    Not Confirmed
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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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    28

    Wyeth Pharmaceuticals Inc

    U.S.A
    Immuno-Oncology 360
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
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    Immuno-Oncology 360
    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 : 1986-12-16

    Application Number : 62717

    Regulatory Info : DISCN

    Registration Country : USA

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    29

    Wyeth Pharmaceuticals Inc

    U.S.A
    Immuno-Oncology 360
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
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    Immuno-Oncology 360
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    NAFCILLIN SODIUM

    Brand Name : UNIPEN

    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 : 1986-12-16

    Application Number : 62717

    Regulatory Info : DISCN

    Registration Country : USA

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    30

    Wyeth Pharmaceuticals Inc

    U.S.A
    Immuno-Oncology 360
    Not Confirmed
    arrow

    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Immuno-Oncology 360
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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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 : 1986-12-16

    Application Number : 62717

    Regulatory Info : DISCN

    Registration Country : USA

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