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Looking for 58-39-9 / Perphenazine API manufacturers, exporters & distributors?

Perphenazine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Perphenazine

Synonyms

58-39-9, Trilafon, Perphenazin, Etaperazine, Perfenazine, Ethaperazine

Cas Number

58-39-9

Unique Ingredient Identifier (UNII)

FTA7XXY4EZ

About Perphenazine

An antipsychotic phenothiazine derivative with actions and uses similar to those of CHLORPROMAZINE.

1446-EP2272537A2 Manufacturers

A 1446-EP2272537A2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1446-EP2272537A2, including repackagers and relabelers. The FDA regulates 1446-EP2272537A2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1446-EP2272537A2 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 1446-EP2272537A2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

1446-EP2272537A2 Suppliers

A 1446-EP2272537A2 supplier is an individual or a company that provides 1446-EP2272537A2 active pharmaceutical ingredient (API) or 1446-EP2272537A2 finished formulations upon request. The 1446-EP2272537A2 suppliers may include 1446-EP2272537A2 API manufacturers, exporters, distributors and traders.

click here to find a list of 1446-EP2272537A2 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

1446-EP2272537A2 USDMF

A 1446-EP2272537A2 DMF (Drug Master File) is a document detailing the whole manufacturing process of 1446-EP2272537A2 active pharmaceutical ingredient (API) in detail. Different forms of 1446-EP2272537A2 DMFs exist exist since differing nations have different regulations, such as 1446-EP2272537A2 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 1446-EP2272537A2 DMF submitted to regulatory agencies in the US is known as a USDMF. 1446-EP2272537A2 USDMF includes data on 1446-EP2272537A2's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 1446-EP2272537A2 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 1446-EP2272537A2 suppliers with USDMF on PharmaCompass.

1446-EP2272537A2 JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The 1446-EP2272537A2 Drug Master File in Japan (1446-EP2272537A2 JDMF) empowers 1446-EP2272537A2 API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the 1446-EP2272537A2 JDMF during the approval evaluation for pharmaceutical products. At the time of 1446-EP2272537A2 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of 1446-EP2272537A2 suppliers with JDMF on PharmaCompass.

1446-EP2272537A2 WC

A 1446-EP2272537A2 written confirmation (1446-EP2272537A2 WC) is an official document issued by a regulatory agency to a 1446-EP2272537A2 manufacturer, verifying that the manufacturing facility of a 1446-EP2272537A2 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 1446-EP2272537A2 APIs or 1446-EP2272537A2 finished pharmaceutical products to another nation, regulatory agencies frequently require a 1446-EP2272537A2 WC (written confirmation) as part of the regulatory process.

click here to find a list of 1446-EP2272537A2 suppliers with Written Confirmation (WC) on PharmaCompass.

1446-EP2272537A2 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 1446-EP2272537A2 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for 1446-EP2272537A2 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 1446-EP2272537A2 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 1446-EP2272537A2 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 1446-EP2272537A2 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of 1446-EP2272537A2 suppliers with NDC on PharmaCompass.

1446-EP2272537A2 GMP

1446-EP2272537A2 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 1446-EP2272537A2 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 1446-EP2272537A2 GMP manufacturer or 1446-EP2272537A2 GMP API supplier for your needs.

1446-EP2272537A2 CoA

A 1446-EP2272537A2 CoA (Certificate of Analysis) is a formal document that attests to 1446-EP2272537A2's compliance with 1446-EP2272537A2 specifications and serves as a tool for batch-level quality control.

1446-EP2272537A2 CoA mostly includes findings from lab analyses of a specific batch. For each 1446-EP2272537A2 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.

1446-EP2272537A2 may be tested according to a variety of international standards, such as European Pharmacopoeia (1446-EP2272537A2 EP), 1446-EP2272537A2 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1446-EP2272537A2 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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