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    01 2ABRAXIS PHARM

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    01

    Actavis Inc

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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PROCAINAMIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

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    Approval Date : 1982-01-01

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    Actavis Inc

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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PROCAINAMIDE HYDROCHLORIDE

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    Approval Date : 1982-01-01

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    03

    Actavis Inc

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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PROCAINAMIDE HYDROCHLORIDE

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    Dosage Strength : 500MG

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    Approval Date : 1982-01-01

    Application Number : 84280

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    04

    Actavis Inc

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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PROCAINAMIDE HYDROCHLORIDE

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    Approval Date : 1982-01-01

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    05

    Actavis Inc

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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PROCAINAMIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 375MG

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    Approval Date : 1982-01-01

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    06

    ANI Pharmaceuticals Inc

    U.S.A
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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PROCAINAMIDE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 1GM

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    Approval Date : 1996-12-13

    Application Number : 40111

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    07

    Bristol Myers Squibb

    U.S.A
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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PRONESTYL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 250MG **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 : 7335

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    08

    Bristol Myers Squibb

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    Regulatory Info : DISCN

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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PRONESTYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 100MG/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 : 7335

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    09

    Bristol Myers Squibb

    U.S.A
    STLE Annual Meeting
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    Regulatory Info : DISCN

    Registration Country : USA

    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PRONESTYL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 500MG **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 : 7335

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    10

    Bristol Myers Squibb

    U.S.A
    STLE Annual Meeting
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    Regulatory Info : DISCN

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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PRONESTYL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 375MG **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 : 7335

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Bristol Myers Squibb

    U.S.A
    STLE Annual Meeting
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    Regulatory Info : DISCN

    Registration Country : USA

    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PRONESTYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 500MG/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 : 7335

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Bristol Myers Squibb

    U.S.A
    STLE Annual Meeting
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    STLE Annual Meeting
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    Regulatory Info : DISCN

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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PRONESTYL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 250MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 17371

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Bristol Myers Squibb

    U.S.A
    STLE Annual Meeting
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    Regulatory Info : DISCN

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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PRONESTYL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 375MG

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    Approval Date : 1982-01-01

    Application Number : 17371

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    14

    Bristol Myers Squibb

    U.S.A
    STLE Annual Meeting
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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PRONESTYL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

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    Approval Date : 1982-01-01

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    15

    IVAX Pharmaceuticals Inc

    U.S.A
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    Brand Name : PROCAINAMIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 375MG

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    Approval Date : 1982-01-01

    Application Number : 84595

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    IVAX Pharmaceuticals Inc

    U.S.A
    American Thoracic Society
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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PROCAINAMIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 250MG

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    Approval Date : 1982-01-01

    Application Number : 84604

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Lannett Company, Inc.

    U.S.A
    STLE Annual Meeting
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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PROCAINAMIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 250MG

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    Approval Date : 1982-01-01

    Application Number : 83693

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Pfizer Inc

    U.S.A
    STLE Annual Meeting
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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PROCANBID

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 1996-01-31

    Application Number : 20545

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Pfizer Inc

    U.S.A
    STLE Annual Meeting
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    Regulatory Info : DISCN

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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PROCANBID

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 1GM

    Packaging :

    Approval Date : 1996-01-31

    Application Number : 20545

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    20

    PANRAY

    Country
    American Thoracic Society
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    PROCAINAMIDE HYDROCHLORIDE

    Brand Name : PROCAPAN

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 250MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 83553

    Regulatory Info : DISCN

    Registration Country : USA

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