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    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.

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    Tobramycin Sulfate

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    01 2Actavis Inc

    02 1Aurobindo Pharma Limited

    03 2B. Braun Medical

    04 1BGP PHARMA ULC

    05 1Baxter Healthcare Corporation

    06 3Bristol Myers Squibb

    07 5Eli Lilly

    08 1Epic Pharma. LLC.

    09 2Fresenius Kabi Austria

    10 4Fresenius Kabi USA

    11 4GLAND PHARMA LIMITED

    12 1Ha Noi CPC1 Pharmaceutical JSC

    13 1Hainan Poly Pharm

    14 5Hikma Pharmaceuticals

    15 8Hospira, Inc.

    16 4IGI Labs, Inc.

    17 1JAMP PHARMA

    18 1JW Pharmaceutical Corporation

    19 2LABORATORIOS NORMON SA

    20 2Meracine

    21 1Montage Laboratories

    22 2Rajasthan Antibiotics

    23 1STERIMAX INC

    24 2Sandoz B2B

    25 1Slate Run Pharmaceuticals

    26 2Teva Pharmaceutical Industries

    27 1Umedica Laboratories

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    29 1XGen Pharmaceuticals

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    01

    Actavis Inc

    Ireland
    FNCE
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    Actavis Inc

    Ireland
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    Regulatory Info : DISCN

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10MG BASE/ML

    Packaging :

    Approval Date : 1989-08-09

    Application Number : 62945

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Actavis Inc

    Ireland
    FNCE
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    Actavis Inc

    Ireland
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    Regulatory Info : DISCN

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML

    Packaging :

    Approval Date : 1989-08-09

    Application Number : 62945

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Eli Lilly

    U.S.A
    FNCE
    Not Confirmed
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    Eli Lilly

    U.S.A
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    FNCE
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    Regulatory Info : DISCN

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : NEBCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50477

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Eli Lilly

    U.S.A
    FNCE
    Not Confirmed
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    Eli Lilly

    U.S.A
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    FNCE
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    Regulatory Info : DISCN

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : NEBCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1.2GM 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 : 50519

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Eli Lilly

    U.S.A
    FNCE
    Not Confirmed
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    Eli Lilly

    U.S.A
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    FNCE
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    Regulatory Info : DISCN

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : NEBCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 62008

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Eli Lilly

    U.S.A
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    Eli Lilly

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : NEBCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10MG BASE/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 62008

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Eli Lilly

    U.S.A
    FNCE
    Not Confirmed
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    Eli Lilly

    U.S.A
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    FNCE
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    Regulatory Info : DISCN

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    TOBRAMYCIN SULFATE

    Brand Name : NEBCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10MG BASE/ML

    Packaging :

    Approval Date : 1987-04-29

    Application Number : 62707

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Fresenius Kabi USA

    U.S.A
    FNCE
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    FNCE
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    Regulatory Info : RX

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1.2GM BASE/VIAL

    Packaging :

    Approval Date : 2004-07-13

    Application Number : 50789

    Regulatory Info : RX

    Registration Country : USA

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    09

    Hikma Pharmaceuticals

    United Kingdom
    FNCE
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    Regulatory Info : DISCN

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10MG BASE/ML

    Packaging :

    Approval Date : 1991-04-26

    Application Number : 63113

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Hikma Pharmaceuticals

    United Kingdom
    FNCE
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    FNCE
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    Regulatory Info : RX

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML

    Packaging :

    Approval Date : 1991-04-26

    Application Number : 63117

    Regulatory Info : RX

    Registration Country : USA

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    11

    Hikma Pharmaceuticals

    United Kingdom
    FNCE
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    FNCE
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    Regulatory Info : DISCN

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML

    Packaging :

    Approval Date : 1991-07-29

    Application Number : 63118

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Hospira, Inc.

    U.S.A
    FNCE
    Not Confirmed
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    Hospira, Inc.

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

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10MG BASE/ML

    Packaging :

    Approval Date : 1991-04-30

    Application Number : 63080

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Hospira, Inc.

    U.S.A
    FNCE
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    FNCE
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    Regulatory Info : DISCN

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 80MG BASE/100ML

    Packaging :

    Approval Date : 1990-07-31

    Application Number : 63081

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Hospira, Inc.

    U.S.A
    FNCE
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    FNCE
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    Regulatory Info : DISCN

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1.2MG BASE/ML

    Packaging :

    Approval Date : 1990-07-31

    Application Number : 63081

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Hospira, Inc.

    U.S.A
    FNCE
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    FNCE
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    Regulatory Info : DISCN

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    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1.6MG BASE/ML

    Packaging :

    Approval Date : 1993-06-02

    Application Number : 63081

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Hospira, Inc.

    U.S.A
    FNCE
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    FNCE
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    Regulatory Info : RX

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML

    Packaging :

    Approval Date : 1991-04-30

    Application Number : 63111

    Regulatory Info : RX

    Registration Country : USA

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    17

    Hospira, Inc.

    U.S.A
    FNCE
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    FNCE
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    Regulatory Info : DISCN

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10MG BASE/ML

    Packaging :

    Approval Date : 1991-04-30

    Application Number : 63112

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Hospira, Inc.

    U.S.A
    FNCE
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    FNCE
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    Regulatory Info : DISCN

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE (PHARMACY BULK)

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1992-05-18

    Application Number : 63116

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    IGI Labs, Inc.

    U.S.A
    FNCE
    Not Confirmed
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    IGI Labs, Inc.

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

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10MG BASE/ML

    Packaging :

    Approval Date : 1994-10-31

    Application Number : 63119

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    Teva Pharmaceutical Industries

    Israel
    FNCE
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    FNCE
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    TOBRAMYCIN SULFATE

    Brand Name : TOBRAMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML

    Packaging :

    Approval Date : 1992-01-30

    Application Number : 63100

    Regulatory Info : DISCN

    Registration Country : USA

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