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    Approved Drug Products containing MolPort-000-883-877 listed in the FDA Orange Book. Original Data : FDA Website

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    Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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    xyz-pharma-m-2024-09-09

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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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    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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    xyz-pharma-m-2024-09-09

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    MolPort-000-883-877

    ACTIVE PHARMA INGREDIENTS

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    PRICE INFORMATION

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    DRUG PRODUCT COMPOSITIONS

    RELATED EXCIPIENT COMPANIES

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    01 10ABBVIE

    02 1ABBOTT

    03 1AMNEAL

    04 3AUROBINDO PHARMA LTD

    05 2CIPLA

    06 4CIPLA LIMITED

    07 1CIPLA LTD

    08 1EMCURE PHARMS LTD

    09 3HETERO LABS LTD III

    10 1HIKMA

    11 1LANNETT CO INC

    12 2LAURUS

    13 2MACLEODS PHARMS LTD

    14 1MATRIX LABS LTD

    15 3MYLAN LABS LTD

    16 2MYLAN PHARMA

    17 2MYLAN PHARMS INC

    18 1NORVIUM BIOSCIENCE

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    01

    ABBVIE

    U.S.A
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    RLD : Yes

    TE Code :

    RITONAVIR

    Brand Name : NORVIR

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 80MG/ML

    Approval Date : 1996-03-01

    Application Number : 20659

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    Abbvie Company Banner

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    02

    ABBVIE

    U.S.A
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    RLD : Yes

    TE Code :

    RITONAVIR

    Brand Name : NORVIR

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1999-06-29

    Application Number : 20945

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    Abbvie Company Banner

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    03

    ABBVIE

    U.S.A
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    RLD : No

    TE Code :

    LOPINAVIR; RITONAVIR

    Brand Name : KALETRA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 133.3MG;33.3MG

    Approval Date : 2000-09-15

    Application Number : 21226

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    Abbvie Company Banner

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    04

    ABBVIE

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    RLD : Yes

    TE Code : AA

    LOPINAVIR; RITONAVIR

    Brand Name : KALETRA

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 80MG/ML;20MG/ML

    Approval Date : 2000-09-15

    Application Number : 21251

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AA

    Abbvie Company Banner

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    05

    ABBVIE

    U.S.A
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    RLD : Yes

    TE Code : AB

    LOPINAVIR; RITONAVIR

    Brand Name : KALETRA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 200MG;50MG

    Approval Date : 2005-10-28

    Application Number : 21906

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

    Abbvie Company Banner

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    06

    ABBVIE

    U.S.A
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    RLD : Yes

    TE Code : AB

    LOPINAVIR; RITONAVIR

    Brand Name : KALETRA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG;25MG

    Approval Date : 2007-11-09

    Application Number : 21906

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

    Abbvie Company Banner

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    07

    ABBVIE

    U.S.A
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    RLD : Yes

    TE Code : AB

    RITONAVIR

    Brand Name : NORVIR

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

    Approval Date : 2010-02-10

    Application Number : 22417

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

    Abbvie Company Banner

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    08

    ABBVIE

    U.S.A
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    RLD : Yes

    TE Code :

    OMBITASVIR; PARITAPREVIR; RITONAVIR

    Brand Name : TECHNIVIE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;75MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 2015-07-24

    Application Number : 207931

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    Abbvie Company Banner

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    09

    ABBVIE

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    RLD : Yes

    TE Code :

    DASABUVIR SODIUM; OMBITASVIR; PARITAPREVIR; RITONAVIR

    Brand Name : VIEKIRA XR

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 200MG BASE;8.33MG;50MG;33.33MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 2016-07-22

    Application Number : 208624

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    Abbvie Company Banner

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    10

    ABBVIE

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    RLD : Yes

    TE Code :

    RITONAVIR

    Brand Name : NORVIR

    Dosage Form : POWDER;ORAL

    Dosage Strength : 100MG/PACKET

    Approval Date : 2017-06-07

    Application Number : 209512

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

    Abbvie Company Banner

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