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  • TABLET;ORAL - 12.5MG;75MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET, EXTENDED RELEASE;ORAL - EQ 200MG BASE;8.33MG;50MG;33.33MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Looking for 1258226-87-7 / Ombitasvir API manufacturers, exporters & distributors?

Ombitasvir manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Ombitasvir API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Ombitasvir manufacturer or Ombitasvir supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ombitasvir manufacturer or Ombitasvir supplier.

PharmaCompass also assists you with knowing the Ombitasvir API Price utilized in the formulation of products. Ombitasvir API Price is not always fixed or binding as the Ombitasvir Price is obtained through a variety of data sources. The Ombitasvir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Ombitasvir

Synonyms

1258226-87-7, Abt-267, Ombitasvir(abt-267), Abt267, Chebi:85183, Abt 267

Cas Number

1258226-87-7

Unique Ingredient Identifier (UNII)

2302768XJ8

About Ombitasvir

Ombitasvir is an orally available inhibitor of the hepatitis C virus (HCV) non-structural protein 5A (NS5A) replication complex, with potential activity against HCV. Upon oral administration and after intracellular uptake, ombitasvir binds to and blocks the activity of the NS5A protein. This results in the disruption of the viral RNA replication complex, blockage of HCV RNA production, and inhibition of viral replication. NS5A, a zinc-binding and proline-rich hydrophilic phosphoprotein, plays a crucial role in HCV RNA replication. HCV is a small, enveloped, single-stranded RNA virus belonging to the Flaviviridae family; HCV infection is associated with the development of hepatocellular carcinoma (HCC).

Ombitasvir Manufacturers

A Ombitasvir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ombitasvir, including repackagers and relabelers. The FDA regulates Ombitasvir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ombitasvir API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Ombitasvir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Ombitasvir Suppliers

A Ombitasvir supplier is an individual or a company that provides Ombitasvir active pharmaceutical ingredient (API) or Ombitasvir finished formulations upon request. The Ombitasvir suppliers may include Ombitasvir API manufacturers, exporters, distributors and traders.

click here to find a list of Ombitasvir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Ombitasvir GMP

Ombitasvir Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of Ombitasvir GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Ombitasvir GMP manufacturer or Ombitasvir GMP API supplier for your needs.

Ombitasvir CoA

A Ombitasvir CoA (Certificate of Analysis) is a formal document that attests to Ombitasvir's compliance with Ombitasvir specifications and serves as a tool for batch-level quality control.

Ombitasvir CoA mostly includes findings from lab analyses of a specific batch. For each Ombitasvir CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Ombitasvir may be tested according to a variety of international standards, such as European Pharmacopoeia (Ombitasvir EP), Ombitasvir JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ombitasvir USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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