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  • TABLET;ORAL - 150MG
  • TABLET;ORAL - 85MG
  • TABLET;ORAL - 150MG;150MG;200MG;300MG
  • TABLET;ORAL - 150MG;150MG;200MG;EQ 10MG BASE

Looking for 697761-98-1 / Elvitegravir API manufacturers, exporters & distributors?

Elvitegravir manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Elvitegravir 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 Elvitegravir manufacturer or Elvitegravir supplier for your needs.

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

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

API | Excipient name

Elvitegravir

Synonyms

697761-98-1, Gs-9137, Jtk-303, Vitekta, Gs 9137, Elvitegravir (gs-9137)

Cas Number

697761-98-1

Unique Ingredient Identifier (UNII)

4GDQ854U53

About Elvitegravir

Elvitegravir is a modified quinolone antibiotic with activity against human immunodeficiency virus 1. Elvitegravir is an inhibitor of viral integrase and retains activity against integrase mutants that are resistant to Raltegravir.

Elvitegravir Manufacturers

A Elvitegravir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Elvitegravir, including repackagers and relabelers. The FDA regulates Elvitegravir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Elvitegravir 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 Elvitegravir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Elvitegravir Suppliers

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

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

Elvitegravir USDMF

A Elvitegravir DMF (Drug Master File) is a document detailing the whole manufacturing process of Elvitegravir active pharmaceutical ingredient (API) in detail. Different forms of Elvitegravir DMFs exist exist since differing nations have different regulations, such as Elvitegravir USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Elvitegravir DMF submitted to regulatory agencies in the US is known as a USDMF. Elvitegravir USDMF includes data on Elvitegravir's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Elvitegravir USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Elvitegravir suppliers with USDMF on PharmaCompass.

Elvitegravir KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a Elvitegravir Drug Master File in Korea (Elvitegravir KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Elvitegravir. The MFDS reviews the Elvitegravir KDMF as part of the drug registration process and uses the information provided in the Elvitegravir KDMF to evaluate the safety and efficacy of the drug.

After submitting a Elvitegravir KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Elvitegravir API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Elvitegravir suppliers with KDMF on PharmaCompass.

Elvitegravir WC

A Elvitegravir written confirmation (Elvitegravir WC) is an official document issued by a regulatory agency to a Elvitegravir manufacturer, verifying that the manufacturing facility of a Elvitegravir active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Elvitegravir APIs or Elvitegravir finished pharmaceutical products to another nation, regulatory agencies frequently require a Elvitegravir WC (written confirmation) as part of the regulatory process.

click here to find a list of Elvitegravir suppliers with Written Confirmation (WC) on PharmaCompass.

Elvitegravir NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Elvitegravir as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Elvitegravir API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Elvitegravir as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Elvitegravir and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Elvitegravir NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Elvitegravir suppliers with NDC on PharmaCompass.

Elvitegravir GMP

Elvitegravir 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 Elvitegravir 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 Elvitegravir GMP manufacturer or Elvitegravir GMP API supplier for your needs.

Elvitegravir CoA

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

Elvitegravir CoA mostly includes findings from lab analyses of a specific batch. For each Elvitegravir 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.

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