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    Cimetidine Hydrochloride

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    01 3ANI Pharmaceuticals Inc

    02 1Chartwell Pharmaceuticals llc

    03 1Cosette Pharma

    04 1Cycle Pharmaceuticals

    05 2ENDO OPERATIONS

    06 1G&W Laboratories

    07 3GSK

    08 11Hospira, Inc.

    09 1Luitpold Pharmaceuticals, Inc.

    10 1PAI Pharmaceutical Associates

    11 2PHARM ASSOC

    12 1PHARMOBEDIENT CNSLTG

    13 1Teva Pharmaceutical Industries

    14 1Vista Pharmaceuticals

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    01

    Chartwell Pharmaceuticals llc

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Chartwell Pharmaceuticals llc

    U.S.A
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 300MG BASE/5ML

    Packaging :

    Approval Date : 1994-12-22

    Application Number : 74251

    Regulatory Info : RX

    Registration Country : USA

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    02

    Cosette Pharma

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Cosette Pharma

    U.S.A
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 300MG BASE/2ML

    Packaging :

    Approval Date : 1997-03-28

    Application Number : 74296

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    G&W Laboratories

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    G&W Laboratories

    U.S.A
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    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 300MG BASE/5ML

    Packaging :

    Approval Date : 1994-06-01

    Application Number : 74176

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    GSK

    United Kingdom
    AMWC Asia-TDAC
    Not Confirmed
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    GSK

    United Kingdom
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : TAGAMET

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 300MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 17924

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    GSK

    United Kingdom
    AMWC Asia-TDAC
    Not Confirmed
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    GSK

    United Kingdom
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : TAGAMET

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 300MG BASE/2ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 17939

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    GSK

    United Kingdom
    AMWC Asia-TDAC
    Not Confirmed
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    GSK

    United Kingdom
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : TAGAMET HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 6MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1985-10-31

    Application Number : 19434

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Hospira, Inc.

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 6MG BASE/ML

    Packaging :

    Approval Date : 1994-12-27

    Application Number : 74269

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Hospira, Inc.

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 300MG BASE/2ML

    Packaging :

    Approval Date : 1995-01-31

    Application Number : 74344

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Hospira, Inc.

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Hospira, Inc.

    U.S.A
    arrow
    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 300MG BASE/2ML

    Packaging :

    Approval Date : 1995-01-31

    Application Number : 74345

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Hospira, Inc.

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Hospira, Inc.

    U.S.A
    arrow
    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 300MG BASE/2ML

    Packaging :

    Approval Date : 1997-03-28

    Application Number : 74412

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Hospira, Inc.

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Hospira, Inc.

    U.S.A
    arrow
    AMWC Asia-TDAC
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 300MG BASE/2ML

    Packaging :

    Approval Date : 1995-01-31

    Application Number : 74422

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Hospira, Inc.

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Hospira, Inc.

    U.S.A
    arrow
    AMWC Asia-TDAC
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 360MG BASE/100ML

    Packaging :

    Approval Date : 1994-12-29

    Application Number : 74468

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Hospira, Inc.

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 480MG BASE/100ML

    Packaging :

    Approval Date : 1994-12-29

    Application Number : 74468

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Hospira, Inc.

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 180MG BASE/100ML

    Packaging :

    Approval Date : 1994-12-29

    Application Number : 74468

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Hospira, Inc.

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 240MG BASE/100ML

    Packaging :

    Approval Date : 1994-12-29

    Application Number : 74468

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Hospira, Inc.

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 90MG BASE/100ML

    Packaging :

    Approval Date : 1994-12-29

    Application Number : 74468

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Luitpold Pharmaceuticals, Inc.

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Luitpold Pharmaceuticals, Inc.

    U.S.A
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 300MG BASE/2ML

    Packaging :

    Approval Date : 1994-12-20

    Application Number : 74353

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Teva Pharmaceutical Industries

    Israel
    AMWC Asia-TDAC
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 300MG BASE/2ML

    Packaging :

    Approval Date : 1997-11-26

    Application Number : 74252

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    ENDO OPERATIONS

    Country
    AMWC Asia-TDAC
    Not Confirmed
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    ENDO OPERATIONS

    Country
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 300MG BASE/2ML

    Packaging :

    Approval Date : 1994-08-31

    Application Number : 74005

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    ENDO OPERATIONS

    Country
    AMWC Asia-TDAC
    Not Confirmed
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    ENDO OPERATIONS

    Country
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    AMWC Asia-TDAC
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CIMETIDINE HYDROCHLORIDE

    Brand Name : CIMETIDINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 300MG BASE/2ML

    Packaging :

    Approval Date : 1996-04-25

    Application Number : 74428

    Regulatory Info : DISCN

    Registration Country : USA

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