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    Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.

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    Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.

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    Acyclovir Sodium

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    01

    AbbVie Inc

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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 50MG BASE/ML

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    Approval Date : 1999-07-26

    Application Number : 75114

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    Dr. Reddy's Laboratories

    India
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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 50MG BASE/ML

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    Approval Date : 2020-06-17

    Application Number : 207919

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    03

    Bristol Myers Squibb

    U.S.A
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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

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    Approval Date : 1998-02-27

    Application Number : 74897

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    04

    Bristol Myers Squibb

    U.S.A
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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 1998-02-27

    Application Number : 74897

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    05

    Chartwell Pharmaceuticals llc

    U.S.A
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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 1997-04-22

    Application Number : 74596

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    Registration Country : USA

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    06

    Chartwell Pharmaceuticals llc

    U.S.A
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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

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    Approval Date : 1997-04-22

    Application Number : 74596

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    07

    Fresenius Kabi USA

    U.S.A
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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 50MG BASE/ML

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    Approval Date : 1998-05-13

    Application Number : 74930

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    08

    GSK

    United Kingdom
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    GSK

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    ACYCLOVIR SODIUM

    Brand Name : ZOVIRAX

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-10-22

    Application Number : 18603

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    Registration Country : USA

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    09

    GSK

    United Kingdom
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    ACYCLOVIR SODIUM

    Brand Name : ZOVIRAX

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1989-06-29

    Application Number : 18603

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    GSK

    United Kingdom
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    GSK

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    ACYCLOVIR SODIUM

    Brand Name : ZOVIRAX

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1983-08-30

    Application Number : 18603

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Hikma Pharmaceuticals

    United Kingdom
    The MedTech Conference
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    Hikma Pharmaceuticals

    United Kingdom
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    Regulatory Info : DISCN

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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR IN SODIUM CHLORIDE 0.9% PRESERVATIVE FREE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1997-12-19

    Application Number : 74885

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Hikma Pharmaceuticals

    United Kingdom
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    Hikma Pharmaceuticals

    United Kingdom
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    Regulatory Info : DISCN

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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR IN SODIUM CHLORIDE 0.9% PRESERVATIVE FREE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1997-12-19

    Application Number : 74885

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Hikma Pharmaceuticals

    United Kingdom
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    United Kingdom
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    Regulatory Info : DISCN

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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1997-10-15

    Application Number : 74913

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Hikma Pharmaceuticals

    United Kingdom
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    Regulatory Info : DISCN

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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1997-10-15

    Application Number : 74913

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Hospira, Inc.

    U.S.A
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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1997-04-22

    Application Number : 74663

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Hospira, Inc.

    U.S.A
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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1997-04-22

    Application Number : 74663

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Hospira, Inc.

    U.S.A
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    Regulatory Info : DISCN

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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 25MG BASE/ML

    Packaging :

    Approval Date : 1997-04-22

    Application Number : 74720

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Hospira, Inc.

    U.S.A
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    Regulatory Info : DISCN

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    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1997-04-22

    Application Number : 74758

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Hospira, Inc.

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1997-04-22

    Application Number : 74758

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    Teva Pharmaceutical Industries

    Israel
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    Israel
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    Regulatory Info : DISCN

    Registration Country : USA

    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1997-08-26

    Application Number : 74969

    Regulatory Info : DISCN

    Registration Country : USA

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