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    Haloperidol Lactate

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    01 1ABRAXIS PHARM

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    04 2Baxter Healthcare Corporation

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    06 1Fosun Pharmaceutical

    07 2Fresenius Kabi USA

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    01

    ABRAXIS PHARM

    U.S.A
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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 1987-01-20

    Application Number : 71187

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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 1988-05-17

    Application Number : 70713

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    03

    Actavis Inc

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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

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    Approval Date : 1988-05-17

    Application Number : 70714

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    04

    Actavis Inc

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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

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    Approval Date : 1988-05-17

    Application Number : 70744

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    05

    Actavis Inc

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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL LACTATE

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 1MG BASE/ML

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    Approval Date : 1995-11-02

    Application Number : 74536

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    06

    Amneal Pharmaceuticals

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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : EQ 2MG BASE/ML

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    Approval Date : 1986-04-11

    Application Number : 70318

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    Baxter Healthcare Corporation

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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2004-08-25

    Application Number : 76791

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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2004-08-25

    Application Number : 76828

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Fosun Pharmaceutical

    China
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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

    Packaging :

    Approval Date : 2004-09-29

    Application Number : 76464

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Fresenius Kabi USA

    U.S.A
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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2001-03-09

    Application Number : 75689

    Regulatory Info : RX

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    11

    GLAND PHARMA LIMITED

    India
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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2004-08-25

    Application Number : 76774

    Regulatory Info : RX

    Registration Country : USA

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    12

    Hikma Pharmaceuticals

    United Kingdom
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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL INTENSOL

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : EQ 2MG BASE/ML

    Packaging :

    Approval Date : 1988-04-12

    Application Number : 72045

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Hikma Pharmaceuticals

    United Kingdom
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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

    Packaging :

    Approval Date : 2001-06-18

    Application Number : 75858

    Regulatory Info : RX

    Registration Country : USA

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    14

    Johnson & Johnson Innovative Medici...

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    HALOPERIDOL LACTATE

    Brand Name : HALDOL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG 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 : 15923

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Lannett Company, Inc.

    U.S.A
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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : EQ 2MG BASE/ML

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    Approval Date : 1993-09-28

    Application Number : 73364

    Regulatory Info : RX

    Registration Country : USA

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    16

    McNeil Consumer Health

    Germany
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    HALOPERIDOL LACTATE

    Brand Name : HALDOL

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : EQ 2MG BASE/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 : 15922

    Regulatory Info : DISCN

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    17

    Morton Grove Pharmaceuticals

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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : EQ 2MG BASE/ML

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    Approval Date : 1986-03-07

    Application Number : 70710

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    Registration Country : USA

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    18

    PHARM ASSOC

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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : EQ 2MG BASE/ML

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    Approval Date : 1993-02-26

    Application Number : 73037

    Regulatory Info : RX

    Registration Country : USA

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    19

    Quad Pharma

    South Africa
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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : Injectable; Injection

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date :

    Application Number : 71082

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    Registration Country : USA

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    20

    SMITH & NEPHEW INC

    Canada
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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

    Packaging :

    Approval Date : 1987-12-14

    Application Number : 70802

    Regulatory Info : DISCN

    Registration Country : USA

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    21

    Solo Pak

    Australia
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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

    Packaging :

    Approval Date : 1987-12-14

    Application Number : 70800

    Regulatory Info : DISCN

    Registration Country : USA

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    22

    Solo Pak

    Australia
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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 1987-12-14

    Application Number : 70801

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    Solo Pak

    Australia
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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

    Packaging :

    Approval Date : 1987-12-14

    Application Number : 70864

    Regulatory Info : DISCN

    Registration Country : USA

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    24

    Specialty Coating Systems, Inc.

    United Kingdom
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    Specialty Coating Systems, Inc.

    United Kingdom
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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : EQ 2MG BASE/ML

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    Approval Date : 1986-06-10

    Application Number : 70726

    Regulatory Info : DISCN

    Registration Country : USA

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    Teva Pharmaceutical Industries

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    HALOPERIDOL LACTATE

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    Approval Date : 1987-08-25

    Application Number : 71015

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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

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    Approval Date : 1988-12-01

    Application Number : 71617

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    HALOPERIDOL LACTATE

    Brand Name : HALOPERIDOL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2001-08-29

    Application Number : 76035

    Regulatory Info : DISCN

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    Approval Date : 2009-09-14

    Application Number : 78347

    Regulatory Info : RX

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    Approval Date : 1993-02-25

    Application Number : 72516

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    Approval Date : 1993-02-25

    Application Number : 72517

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