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    Pentobarbital Sodium

    ACTIVE PHARMA INGREDIENTS

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

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    01 1ANABOLIC

    02 1BPI LABS

    03 2ELKINS SINN

    04 3EPIC PHARMA LLC

    05 1EVERYLIFE

    06 1HALSEY

    07 1HIKMA

    08 2IVAX SUB TEVA PHARMS

    09 2LANNETT

    10 1NEXGEN PHARMA INC

    11 1PARKE DAVIS

    12 1PERRIGO

    13 1PUREPAC PHARM

    14 1RISING

    15 1SAGENT PHARMS INC

    16 5SCIEGEN PHARMS INC

    17 1VALEANT PHARM INTL

    18 2VITARINE

    19 1WATSON LABS

    20 1WHITEWORTH TOWN PLSN

    21 2WYETH AYERST

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    01

    EPIC PHARMA LLC

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    EPIC PHARMA LLC

    U.S.A
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    RLD : No

    TE Code :

    PENTOBARBITAL SODIUM

    Brand Name : NEMBUTAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 83245

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    EVERYLIFE

    United Kingdom
    Fi Europe 2024
    Not Confirmed
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    EVERYLIFE

    United Kingdom
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    RLD : No

    TE Code :

    PENTOBARBITAL SODIUM

    Brand Name : SODIUM PENTOBARBITAL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 83259

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    RISING

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    RISING

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    RLD : Yes

    TE Code : AP

    PENTOBARBITAL SODIUM

    Brand Name : NEMBUTAL SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/ML

    Approval Date : 1982-01-01

    Application Number : 83246

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    04

    SCIEGEN PHARMS INC

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    SCIEGEN PHARMS INC

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    RLD : No

    TE Code :

    PENTOBARBITAL

    Brand Name : NEMBUTAL

    Dosage Form : ELIXIR;ORAL

    Dosage Strength : 18.2MG/5ML

    Approval Date : 1982-01-01

    Application Number : 83244

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    SCIEGEN PHARMS INC

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    SCIEGEN PHARMS INC

    U.S.A
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    Fi Europe 2024
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    RLD : No

    TE Code :

    PENTOBARBITAL SODIUM

    Brand Name : NEMBUTAL

    Dosage Form : SUPPOSITORY;RECTAL

    Dosage Strength : 30MG

    Approval Date : 1982-01-25

    Application Number : 83247

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    SCIEGEN PHARMS INC

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    SCIEGEN PHARMS INC

    U.S.A
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    Fi Europe 2024
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    RLD : No

    TE Code :

    PENTOBARBITAL SODIUM

    Brand Name : NEMBUTAL

    Dosage Form : SUPPOSITORY;RECTAL

    Dosage Strength : 60MG

    Approval Date : 1982-01-25

    Application Number : 83247

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    SCIEGEN PHARMS INC

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    SCIEGEN PHARMS INC

    U.S.A
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    Fi Europe 2024
    Not Confirmed
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    RLD : No

    TE Code :

    PENTOBARBITAL SODIUM

    Brand Name : NEMBUTAL

    Dosage Form : SUPPOSITORY;RECTAL

    Dosage Strength : 120MG

    Approval Date : 1982-01-25

    Application Number : 83247

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    SCIEGEN PHARMS INC

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    SCIEGEN PHARMS INC

    U.S.A
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    Fi Europe 2024
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    RLD : No

    TE Code :

    PENTOBARBITAL SODIUM

    Brand Name : NEMBUTAL

    Dosage Form : SUPPOSITORY;RECTAL

    Dosage Strength : 200MG

    Approval Date : 1982-01-25

    Application Number : 83247

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    09

    WYETH AYERST

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    WYETH AYERST

    U.S.A
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    Fi Europe 2024
    Not Confirmed
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    RLD : No

    TE Code :

    PENTOBARBITAL SODIUM

    Brand Name : SODIUM PENTOBARBITAL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 83239

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    WYETH AYERST

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    WYETH AYERST

    U.S.A
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    Fi Europe 2024
    Not Confirmed
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    RLD : No

    TE Code :

    PENTOBARBITAL SODIUM

    Brand Name : SODIUM PENTOBARBITAL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/ML

    Approval Date : 1982-01-01

    Application Number : 83261

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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