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    01 1ABRAXIS PHARM

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    03 1ANI Pharmaceuticals Inc

    04 1APOZEAL PHARMS

    05 1Ajanta Pharma Limited

    06 2Amneal Pharmaceuticals

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    01

    ABRAXIS PHARM

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    ABRAXIS PHARM

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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 250MG/ML

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    Approval Date : 1986-06-17

    Application Number : 70522

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Amneal Pharmaceuticals

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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

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    Approval Date : 2019-11-26

    Application Number : 212492

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    03

    Amneal Pharmaceuticals

    U.S.A
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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 0.25GM/ML

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    Approval Date : 2019-08-23

    Application Number : 212780

    Regulatory Info : RX

    Registration Country : USA

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    04

    ANI Pharmaceuticals Inc

    U.S.A
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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

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    Approval Date : 2020-12-14

    Application Number : 211629

    Regulatory Info : DISCN

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    05

    Baxter Healthcare Corporation

    U.S.A
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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 250MG/ML

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    Approval Date : 1982-10-29

    Application Number : 18590

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Epic Pharma. LLC.

    U.S.A
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    AMINOCAPROIC ACID

    Brand Name : AMICAR

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 250MG/ML **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 : 15229

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Epic Pharma. LLC.

    U.S.A
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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 0.25GM/ML

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    Approval Date : 1998-09-02

    Application Number : 74759

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Hikma Pharmaceuticals

    United Kingdom
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    AMINOCAPROIC ACID

    Brand Name : AMICAR

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 15197

    Regulatory Info : RX

    Registration Country : USA

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    09

    Hikma Pharmaceuticals

    United Kingdom
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    AMINOCAPROIC ACID

    Brand Name : AMICAR

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1GM

    Packaging :

    Approval Date : 2004-06-24

    Application Number : 15197

    Regulatory Info : RX

    Registration Country : USA

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    10

    Hikma Pharmaceuticals

    United Kingdom
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    AMINOCAPROIC ACID

    Brand Name : AMICAR

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 0.25GM/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 15230

    Regulatory Info : RX

    Registration Country : USA

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    11

    Hikma Pharmaceuticals

    United Kingdom
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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 2001-05-24

    Application Number : 75602

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Hospira, Inc.

    U.S.A
    The Aesthetic Show
    Not Confirmed
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    Hospira, Inc.

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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 250MG/ML

    Packaging :

    Approval Date : 1987-03-09

    Application Number : 70010

    Regulatory Info : RX

    Registration Country : USA

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    13

    Hospira, Inc.

    U.S.A
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    U.S.A
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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 250MG/ML

    Packaging :

    Approval Date : 1988-06-16

    Application Number : 70888

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Luitpold Pharmaceuticals, Inc.

    U.S.A
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    U.S.A
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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 250MG/ML

    Packaging :

    Approval Date : 1987-12-01

    Application Number : 71192

    Regulatory Info : RX

    Registration Country : USA

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    15

    Quad Pharma

    South Africa
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    Quad Pharma

    South Africa
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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID

    Dosage Form : Injectable; Injection

    Dosage Strength : 250MG/ML

    Packaging :

    Approval Date :

    Application Number : 70694

    Regulatory Info :

    Registration Country : USA

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    16

    Sunny Pharmtech

    Taiwan
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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 2018-11-27

    Application Number : 209060

    Regulatory Info : RX

    Registration Country : USA

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    17

    Sunny Pharmtech

    Taiwan
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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1GM

    Packaging :

    Approval Date : 2018-11-27

    Application Number : 209060

    Regulatory Info : RX

    Registration Country : USA

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    18

    Trupharma

    U.S.A
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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 0.25GM/ML

    Packaging :

    Approval Date : 2020-08-11

    Application Number : 212494

    Regulatory Info : RX

    Registration Country : USA

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    19

    Vista Pharmaceuticals

    India
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    India
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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 0.25GM/ML

    Packaging :

    Approval Date : 2020-02-26

    Application Number : 212814

    Regulatory Info : DISCN

    Registration Country : USA

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    ADAPTIS

    Country
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    ADAPTIS

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    AMINOCAPROIC ACID

    Brand Name : AMINOCAPROIC ACID

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 2021-06-14

    Application Number : 212110

    Regulatory Info : DISCN

    Registration Country : USA

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