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    ACTIVE PHARMA INGREDIENTS

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    01 2ANI Pharmaceuticals Inc

    02 6Actavis Inc

    03 2Antibiotice

    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 2ONESOURCE SPECIALTY

    13 3Piramal Enterprises Limited

    14 2Reyoung pharmaceutical

    15 3Sagent Pharmaceuticals

    16 7Sandoz B2B

    17 1Teva Pharmaceutical Industries

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    01

    Baxter Healthcare Corporation

    U.S.A
    ELCC
    Not Confirmed
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    Baxter Healthcare Corporation

    U.S.A
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    ELCC
    Not Confirmed
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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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    02

    Baxter Healthcare Corporation

    U.S.A
    ELCC
    Not Confirmed
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    Baxter Healthcare Corporation

    U.S.A
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    ELCC
    Not Confirmed
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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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    03

    Bristol Myers Squibb

    U.S.A
    ELCC
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ELCC
    Not Confirmed
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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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    04

    Bristol Myers Squibb

    U.S.A
    ELCC
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ELCC
    Not Confirmed
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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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    05

    Bristol Myers Squibb

    U.S.A
    ELCC
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ELCC
    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 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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    06

    Bristol Myers Squibb

    U.S.A
    ELCC
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ELCC
    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 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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    07

    Bristol Myers Squibb

    U.S.A
    ELCC
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ELCC
    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 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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    08

    Bristol Myers Squibb

    U.S.A
    ELCC
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ELCC
    Not Confirmed
    • fda
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    Virtual Booth Virtual Booth
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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

    blank

    Portfolio PDF

    Product Web Link

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    09

    Bristol Myers Squibb

    U.S.A
    ELCC
    Not Confirmed
    arrow

    Bristol Myers Squibb

    U.S.A
    arrow
    ELCC
    Not Confirmed
    • fda
    • EDQM
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    Flag U.S.A
    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 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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    Digital Content

    Website

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    10

    Bristol Myers Squibb

    U.S.A
    ELCC
    Not Confirmed
    arrow

    Bristol Myers Squibb

    U.S.A
    arrow
    ELCC
    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 U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    11

    Bristol Myers Squibb

    U.S.A
    ELCC
    Not Confirmed
    arrow

    Bristol Myers Squibb

    U.S.A
    arrow
    ELCC
    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

    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

    Product Web Link

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    Digital Content

    Website

    Corporate PDF

    12

    Bristol Myers Squibb

    U.S.A
    ELCC
    Not Confirmed
    arrow

    Bristol Myers Squibb

    U.S.A
    arrow
    ELCC
    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

    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

    blank

    Portfolio PDF

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    13

    GSK

    United Kingdom
    ELCC
    Not Confirmed
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    GSK

    United Kingdom
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    ELCC
    Not Confirmed
    • fda
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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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    14

    GSK

    United Kingdom
    ELCC
    Not Confirmed
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    GSK

    United Kingdom
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    ELCC
    Not Confirmed
    • fda
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    Virtual Booth Virtual Booth
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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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    15

    GSK

    United Kingdom
    ELCC
    Not Confirmed
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    GSK

    United Kingdom
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    ELCC
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    16

    GSK

    United Kingdom
    ELCC
    Not Confirmed
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    GSK

    United Kingdom
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    ELCC
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    17

    GSK

    United Kingdom
    ELCC
    Not Confirmed
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    GSK

    United Kingdom
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    ELCC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    18

    GSK

    United Kingdom
    ELCC
    Not Confirmed
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    GSK

    United Kingdom
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    ELCC
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    19

    GSK

    United Kingdom
    ELCC
    Not Confirmed
    arrow

    GSK

    United Kingdom
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    ELCC
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    20

    Sandoz B2B

    Switzerland
    ELCC
    Not Confirmed
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    Sandoz B2B

    Switzerland
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    ELCC
    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 250MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61490

    Regulatory Info : DISCN

    Registration Country : USA

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.