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    Approved Drug Products containing Acyclovir Sodium listed in the FDA Orange Book. Original Data : FDA Website

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    Bora Pharmaceuticals- Making success more certain.

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

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    Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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    Acyclovir Sodium

    ACTIVE PHARMA INGREDIENTS

    PRICE INFORMATION

    FINISHED DOSAGE FORMULATIONS

    DIGITAL CONTENT

    GLOBAL SALES INFORMATION

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

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    01 1ABBVIE

    02 1DR REDDYS

    03 2APOTHECON

    04 2CHARTWELL INJECTABLE

    05 1EUGIA PHARMA

    06 4EUROHLTH INTL SARL

    07 3FRESENIUS KABI USA

    08 3GLAXOSMITHKLINE

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    11 2NORVIUM BIOSCIENCE

    12 1SLATE RUN PHARMA

    13 3TEVA PARENTERAL

    14 3ZYDUS PHARMS

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    01

    ABBVIE

    U.S.A
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    FNCE 2024
    Not Confirmed
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    RLD : No

    TE Code :

    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 50MG BASE/ML

    Approval Date : 1999-07-26

    Application Number : 75114

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    DR REDDYS

    India
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    Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    RLD : No

    TE Code :

    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 50MG BASE/ML

    Approval Date : 2020-06-17

    Application Number : 207919

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    Dr Reddy Company Banner

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    03

    CHARTWELL INJECTABLE

    U.S.A
    FNCE 2024
    Not Confirmed
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    CHARTWELL INJECTABLE

    U.S.A
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    RLD : No

    TE Code :

    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Approval Date : 1997-04-22

    Application Number : 74596

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    CHARTWELL INJECTABLE

    U.S.A
    FNCE 2024
    Not Confirmed
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    CHARTWELL INJECTABLE

    U.S.A
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    RLD : No

    TE Code :

    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Approval Date : 1997-04-22

    Application Number : 74596

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    GLAXOSMITHKLINE

    United Kingdom
    FNCE 2024
    Not Confirmed
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    GLAXOSMITHKLINE

    United Kingdom
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    FNCE 2024
    Not Confirmed
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    RLD : Yes

    TE Code :

    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**

    Approval Date : 1982-10-22

    Application Number : 18603

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    06

    GLAXOSMITHKLINE

    United Kingdom
    FNCE 2024
    Not Confirmed
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    GLAXOSMITHKLINE

    United Kingdom
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    FNCE 2024
    Not Confirmed
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    RLD : Yes

    TE Code :

    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**

    Approval Date : 1989-06-29

    Application Number : 18603

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    07

    GLAXOSMITHKLINE

    United Kingdom
    FNCE 2024
    Not Confirmed
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    GLAXOSMITHKLINE

    United Kingdom
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    FNCE 2024
    Not Confirmed
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    RLD : Yes

    TE Code :

    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**

    Approval Date : 1983-08-30

    Application Number : 18603

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    08

    HOSPIRA

    U.S.A
    FNCE 2024
    Not Confirmed
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    HOSPIRA

    U.S.A
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    FNCE 2024
    Not Confirmed
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    RLD : No

    TE Code :

    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Approval Date : 1997-04-22

    Application Number : 74663

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    09

    HOSPIRA

    U.S.A
    FNCE 2024
    Not Confirmed
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    HOSPIRA

    U.S.A
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    FNCE 2024
    Not Confirmed
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    RLD : No

    TE Code :

    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Approval Date : 1997-04-22

    Application Number : 74663

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    10

    HOSPIRA

    U.S.A
    FNCE 2024
    Not Confirmed
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    HOSPIRA

    U.S.A
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    FNCE 2024
    Not Confirmed
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    RLD : No

    TE Code :

    ACYCLOVIR SODIUM

    Brand Name : ACYCLOVIR SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 25MG BASE/ML

    Approval Date : 1997-04-22

    Application Number : 74720

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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