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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.

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    Oxacillin Sodium

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    01 2ANI Pharmaceuticals Inc

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    04 3Aurobindo Pharma Limited

    05 2Baxter Healthcare Corporation

    06 10Bristol Myers Squibb

    07 6ELKINS SINN

    08 3Fresenius Kabi USA

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    11 5Istituto Biochimico Italiano Giovanni Lorenzini SpA

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    01

    Baxter Healthcare Corporation

    U.S.A
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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

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    Approval Date : 1989-10-26

    Application Number : 50640

    Regulatory Info : RX

    Registration Country : USA

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    02

    Baxter Healthcare Corporation

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    Regulatory Info : RX

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    OXACILLIN SODIUM

    Brand Name : BACTOCILL IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML

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    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
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    Regulatory Info : DISCN

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    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

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    Regulatory Info : DISCN

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    OXACILLIN SODIUM

    Brand Name : PROSTAPHLIN

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : EQ 250MG BASE/5ML

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    Approval Date : 1982-01-01

    Application Number : 50194

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Bristol Myers Squibb

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    Regulatory Info : DISCN

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    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**

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    Approval Date : 1982-01-01

    Application Number : 50195

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Bristol Myers Squibb

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    Regulatory Info : DISCN

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    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**

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    Approval Date : 1982-01-01

    Application Number : 50195

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Bristol Myers Squibb

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    Regulatory Info : DISCN

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    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

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    Regulatory Info : DISCN

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    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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    09

    Bristol Myers Squibb

    U.S.A
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    Regulatory Info : DISCN

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    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

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    10

    Bristol Myers Squibb

    U.S.A
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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 : 61450

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Bristol Myers Squibb

    U.S.A
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    Regulatory Info : DISCN

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    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

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    12

    Bristol Myers Squibb

    U.S.A
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    Regulatory Info : DISCN

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    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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    13

    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 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
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    Regulatory Info : DISCN

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    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
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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**

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    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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    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**

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    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 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
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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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    19

    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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    20

    Sandoz B2B

    Switzerland
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    Switzerland
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    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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