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  • POWDER;INHALATION - 0.05MG/INH;EQ 0.025MG BASE/INH
  • POWDER;INHALATION - 0.1MG/INH;EQ 0.025MG BASE/INH
  • POWDER;INHALATION - 0.2MG/INH;EQ 0.025MG BASE/INH

Looking for 503070-58-4 / Vilanterol Trifenatate API manufacturers, exporters & distributors?

Vilanterol Trifenatate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Vilanterol Trifenatate

Synonyms

503070-58-4, Vilanterol trifenate, Vilanterol (trifenatate), Gw642444m, Unii-40aho2c6dg, Chebi:75040

Cas Number

503070-58-4

Unique Ingredient Identifier (UNII)

40AHO2C6DG

Vilanterol Manufacturers

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

Vilanterol Suppliers

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

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

Vilanterol USDMF

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

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

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

Vilanterol KDMF

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

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

After submitting a Vilanterol 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 Vilanterol API can apply through the Korea Drug Master File (KDMF).

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

Vilanterol WC

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

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

Vilanterol 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 Vilanterol as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Vilanterol 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 Vilanterol 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 Vilanterol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Vilanterol NDC to their finished compounded human drug products, they may choose to do so.

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

Vilanterol GMP

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

Vilanterol CoA

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

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

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