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    Dr. Reddy's Laboratories

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    OXYTOCIN

    Brand Name : OXYTOCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10USP UNITS/ML (10USP UNITS/ML)

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    Approval Date : 2008-01-24

    Application Number : 77453

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    02

    Ever Pharma

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    Oxytocin

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    Dr. Reddy's Laboratories

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    OXYTOCIN

    Brand Name : OXYTOCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 100USP UNITS/10ML (10USP UNITS/ML)

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    Approval Date : 2008-01-24

    Application Number : 77453

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Ever Pharma

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    Oxytocin

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    Dosage Form : Solution for Injection

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    05

    Abbott Laboratories

    U.S.A
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    OXYTOCIN

    Brand Name : OXYTOCIN 5 USP UNITS IN DEXTROSE 5%

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1USP UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1985-03-29

    Application Number : 19185

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    Registration Country : USA

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    06

    Abbott Laboratories

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    OXYTOCIN

    Brand Name : OXYTOCIN 20 USP UNITS IN DEXTROSE 5%

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 2USP UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1985-03-29

    Application Number : 19185

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    Registration Country : USA

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    07

    Abbott Laboratories

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    OXYTOCIN

    Brand Name : OXYTOCIN 10 USP UNITS IN DEXTROSE 5%

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 2USP UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1985-03-29

    Application Number : 19185

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    Registration Country : USA

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    08

    Abbott Laboratories

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    OXYTOCIN

    Brand Name : OXYTOCIN 10 USP UNITS IN DEXTROSE 5%

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1USP UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1985-03-29

    Application Number : 19185

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Fresenius Kabi USA

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    Regulatory Info : RX

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    OXYTOCIN

    Brand Name : OXYTOCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10USP UNITS/ML (10USP UNITS/ML)

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18248

    Regulatory Info : RX

    Registration Country : USA

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    10

    Fresenius Kabi USA

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    Regulatory Info : RX

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    OXYTOCIN

    Brand Name : OXYTOCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 100USP UNITS/10ML (10USP UNITS/ML)

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18248

    Regulatory Info : RX

    Registration Country : USA

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    11

    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : RX

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    OXYTOCIN

    Brand Name : OXYTOCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 300USP UNITS/30ML (10USP UNITS/ML)

    Packaging :

    Approval Date : 2007-07-27

    Application Number : 18248

    Regulatory Info : RX

    Registration Country : USA

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    12

    Hikma Pharmaceuticals

    United Kingdom
    Iran Expo
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    United Kingdom
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    Regulatory Info : RX

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    OXYTOCIN

    Brand Name : OXYTOCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10USP UNITS/ML (10USP UNITS/ML)

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18243

    Regulatory Info : RX

    Registration Country : USA

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    13

    Hikma Pharmaceuticals

    United Kingdom
    Iran Expo
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    Hikma Pharmaceuticals

    United Kingdom
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    Regulatory Info : RX

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    OXYTOCIN

    Brand Name : OXYTOCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 100USP UNITS/10ML (10USP UNITS/ML)

    Packaging :

    Approval Date : 2007-01-10

    Application Number : 18243

    Regulatory Info : RX

    Registration Country : USA

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    14

    Novartis Pharmaceuticals Corporatio...

    Switzerland
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    Switzerland
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    OXYTOCIN

    Brand Name : SYNTOCINON

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10USP UNITS/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18245

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Sagent Pharmaceuticals

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    OXYTOCIN

    Brand Name : OXYTOCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10USP UNITS/ML (10USP UNITS/ML)

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    Approval Date : 2018-07-13

    Application Number : 91676

    Regulatory Info : RX

    Registration Country : USA

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    16

    Sagent Pharmaceuticals

    U.S.A
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    Brand Name : OXYTOCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 100USP UNITS/10ML (10USP UNITS/ML)

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    Approval Date : 2018-07-13

    Application Number : 91676

    Regulatory Info : RX

    Registration Country : USA

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    17

    Travere Therapeutics

    U.S.A
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    OXYTOCIN

    Brand Name : SYNTOCINON

    Dosage Form : SOLUTION;NASAL

    Dosage Strength : 40USP UNITS/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 12285

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    ENDO OPERATIONS

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    OXYTOCIN

    Brand Name : PITOCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10USP UNITS/ML (10USP UNITS/ML)

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18261

    Regulatory Info : RX

    Registration Country : USA

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    19

    ENDO OPERATIONS

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    Iran Expo
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    OXYTOCIN

    Brand Name : PITOCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 100USP UNITS/10ML (10USP UNITS/ML)

    Packaging :

    Approval Date : 2007-07-27

    Application Number : 18261

    Regulatory Info : RX

    Registration Country : USA

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    20

    ENDO OPERATIONS

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    Iran Expo
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    OXYTOCIN

    Brand Name : PITOCIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 500USP UNITS/50ML (10USP UNITS/ML)

    Packaging :

    Approval Date : 2012-09-05

    Application Number : 18261

    Regulatory Info : RX

    Registration Country : USA

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