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    Suanfarma, at the Core of a Better Life.

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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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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.

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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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    Oxacillin Sodium

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

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    01 2ANI Pharmaceuticals Inc

    02 6Actavis Inc

    03 2Antibiotice SA

    04 3Aurobindo Pharma Limited

    05 2Baxter Healthcare Corporation

    06 10Bristol Myers Squibb

    07 6ELKINS SINN

    08 3Fresenius Kabi USA

    09 12GSK

    10 2Hospira, Inc.

    11 5Istituto Biochimico Italiano Giovanni Lorenzini SpA

    12 3Piramal Enterprises Limited

    13 2Reyoung pharmaceutical

    14 2STERISCIENCE SPECLTS

    15 3Sagent Pharmaceuticals

    16 7Sandoz B2B

    17 1Teva Pharmaceutical Industries

    18 3Wockhardt

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    01

    ANI Pharmaceuticals Inc

    U.S.A
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    ANI Pharmaceuticals Inc

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    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 250MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 62222

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    ANI Pharmaceuticals Inc

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    ANI Pharmaceuticals Inc

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    Regulatory Info : DISCN

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    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 62222

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Baxter Healthcare Corporation

    U.S.A
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    Baxter Healthcare Corporation

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    Regulatory Info : RX

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : BACTOCILL IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20MG BASE/ML

    Packaging :

    Approval Date : 1989-10-26

    Application Number : 50640

    Regulatory Info : RX

    Registration Country : USA

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    04

    Baxter Healthcare Corporation

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    Regulatory Info : RX

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : BACTOCILL IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML

    Packaging :

    Approval Date : 1989-10-26

    Application Number : 50640

    Regulatory Info : RX

    Registration Country : USA

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    05

    Bristol Myers Squibb

    U.S.A
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    Bristol Myers Squibb

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    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : PROSTAPHLIN

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50118

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Bristol Myers Squibb

    U.S.A
    PharmaVenue
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    Bristol Myers Squibb

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : PROSTAPHLIN

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : EQ 250MG BASE/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50194

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Bristol Myers Squibb

    U.S.A
    PharmaVenue
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    Bristol Myers Squibb

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    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 250MG 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 : 50195

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Bristol Myers Squibb

    U.S.A
    PharmaVenue
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    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 : 50195

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Bristol Myers Squibb

    U.S.A
    PharmaVenue
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    PharmaVenue
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    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    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 : 50195

    Regulatory Info : DISCN

    Registration Country : USA

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    Portfolio PDF

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    10

    Bristol Myers Squibb

    U.S.A
    PharmaVenue
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    PharmaVenue
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    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 : 50195

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Bristol Myers Squibb

    U.S.A
    PharmaVenue
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    PharmaVenue
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    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    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 : 50195

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

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    12

    Bristol Myers Squibb

    U.S.A
    PharmaVenue
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    PharmaVenue
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    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61450

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

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    13

    Bristol Myers Squibb

    U.S.A
    PharmaVenue
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    PharmaVenue
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    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 250MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61450

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

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    14

    Bristol Myers Squibb

    U.S.A
    PharmaVenue
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : EQ 250MG BASE/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61457

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    GSK

    United Kingdom
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    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : BACTOCILL

    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 : 1982-03-26

    Application Number : 61334

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    GSK

    United Kingdom
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    GSK

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    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : BACTOCILL

    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 : 1982-03-26

    Application Number : 61334

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    GSK

    United Kingdom
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    Regulatory Info : DISCN

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    OXACILLIN SODIUM

    Brand Name : BACTOCILL

    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 : 1982-03-26

    Application Number : 61334

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    GSK

    United Kingdom
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    Regulatory Info : DISCN

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    OXACILLIN SODIUM

    Brand Name : BACTOCILL

    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 : 1982-03-26

    Application Number : 61334

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    GSK

    United Kingdom
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    Regulatory Info : DISCN

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    OXACILLIN SODIUM

    Brand Name : BACTOCILL

    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 : 61334

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    GSK

    United Kingdom
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    Regulatory Info : DISCN

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    OXACILLIN SODIUM

    Brand Name : BACTOCILL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 250MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61336

    Regulatory Info : DISCN

    Registration Country : USA

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    21

    GSK

    United Kingdom
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    Regulatory Info : DISCN

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    OXACILLIN SODIUM

    Brand Name : BACTOCILL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61336

    Regulatory Info : DISCN

    Registration Country : USA

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    22

    GSK

    United Kingdom
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    OXACILLIN SODIUM

    Brand Name : BACTOCILL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 250MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 62241

    Regulatory Info : DISCN

    Registration Country : USA

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    23

    GSK

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    Regulatory Info : DISCN

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    OXACILLIN SODIUM

    Brand Name : BACTOCILL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 62241

    Regulatory Info : DISCN

    Registration Country : USA

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    24

    GSK

    United Kingdom
    PharmaVenue
    Not Confirmed
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    GSK

    United Kingdom
    arrow
    PharmaVenue
    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

    OXACILLIN SODIUM

    Brand Name : BACTOCILL

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : EQ 250MG BASE/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 62321

    Regulatory Info : DISCN

    Registration Country : USA

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    25

    Sandoz B2B

    Switzerland
    PharmaVenue
    Not Confirmed
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    Sandoz B2B

    Switzerland
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    PharmaVenue
    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 Switzerland
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 250MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61490

    Regulatory Info : DISCN

    Registration Country : USA

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    Product Web Link

    Virtual Booth

    Digital Content

    Website

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    26

    Sandoz B2B

    Switzerland
    PharmaVenue
    Not Confirmed
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    Sandoz B2B

    Switzerland
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    PharmaVenue
    Not Confirmed
    • fda
    • EDQM
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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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    Flag Switzerland
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61490

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    27

    Sandoz B2B

    Switzerland
    PharmaVenue
    Not Confirmed
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    Sandoz B2B

    Switzerland
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    PharmaVenue
    Not Confirmed
    • fda
    • EDQM
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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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    Flag Switzerland
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61490

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

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    Digital Content

    Website

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    28

    Sandoz B2B

    Switzerland
    PharmaVenue
    Not Confirmed
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    Sandoz B2B

    Switzerland
    arrow
    PharmaVenue
    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 Switzerland
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61490

    Regulatory Info : DISCN

    Registration Country : USA

    blank

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    Digital Content

    Website

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    29

    Sandoz B2B

    Switzerland
    PharmaVenue
    Not Confirmed
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    Sandoz B2B

    Switzerland
    arrow
    PharmaVenue
    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 Switzerland
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10GM BASE/VIAL

    Packaging :

    Approval Date : 1991-05-09

    Application Number : 61490

    Regulatory Info : DISCN

    Registration Country : USA

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    30

    Teva Pharmaceutical Industries

    Israel
    PharmaVenue
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
    arrow
    PharmaVenue
    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 Israel
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    OXACILLIN SODIUM

    Brand Name : OXACILLIN SODIUM

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : EQ 250MG BASE/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 62252

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF