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

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    xyz-pharma-m-2024-10-07

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    Nafcillin Sodium

    ACTIVE PHARMA INGREDIENTS

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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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    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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    02

    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
    Antibody Engineering
    Not Confirmed
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    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
    Antibody Engineering
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    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
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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

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61999

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    GSK

    United Kingdom
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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
    Antibody Engineering
    Not Confirmed
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    GSK

    United Kingdom
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    Antibody Engineering
    Not Confirmed
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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
    Antibody Engineering
    Not Confirmed
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    GSK

    United Kingdom
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    Antibody Engineering
    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
    Antibody Engineering
    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
    Antibody Engineering
    Not Confirmed
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    GSK

    United Kingdom
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    Antibody Engineering
    Not Confirmed
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    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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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 : 1986-12-19

    Application Number : 62755

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Sandoz B2B

    Switzerland
    Antibody Engineering
    Not Confirmed
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    Sandoz B2B

    Switzerland
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    Antibody Engineering
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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
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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

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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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    Sandoz B2B

    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 10GM BASE/VIAL

    Packaging :

    Approval Date : 1984-08-02

    Application Number : 62527

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Sandoz B2B

    Switzerland
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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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    Sandoz B2B

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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
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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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    20

    Wyeth Pharmaceuticals Inc

    U.S.A
    Antibody Engineering
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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
    Antibody Engineering
    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 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
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    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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    Wyeth Pharmaceuticals Inc

    U.S.A
    Antibody Engineering
    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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    Wyeth Pharmaceuticals Inc

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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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    Portfolio PDF

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    Virtual Booth

    Digital Content

    Website

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    25

    Wyeth Pharmaceuticals Inc

    U.S.A
    Antibody Engineering
    Not Confirmed
    arrow

    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

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    26

    Wyeth Pharmaceuticals Inc

    U.S.A
    Antibody Engineering
    Not Confirmed
    arrow

    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

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    Website

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    27

    Wyeth Pharmaceuticals Inc

    U.S.A
    Antibody Engineering
    Not Confirmed
    arrow

    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

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    28

    Wyeth Pharmaceuticals Inc

    U.S.A
    Antibody Engineering
    Not Confirmed
    arrow

    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

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    Digital Content

    Website

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    29

    Wyeth Pharmaceuticals Inc

    U.S.A
    Antibody Engineering
    Not Confirmed
    arrow

    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    30

    Wyeth Pharmaceuticals Inc

    U.S.A
    Antibody Engineering
    Not Confirmed
    arrow

    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF