Close
4

Athena Athena

X

Find Diclazuril manufacturers, exporters & distributors on PharmaCompass

PharmaCompass
API SUPPLIERS
API Suppliers

API Suppliers

US DMFs Filed

US DMFs Filed

CEP/COS Certifications

CEP/COS Certifications

JDMFs Filed

JDMFs Filed

0

Other Certificates

Other Certificates

0

Other Suppliers

Other Suppliers

API REF. PRICE (USD / KG)
544
INTERMEDIATES
DOSSIERS // FDF
USA (Orange Book)

USA (Orange Book)

0

Europe

Europe

0

Canada

Canada

Australia

Australia

0

South Africa

South Africa

0

Uploaded Dossiers

Uploaded Dossiers

0

GLOBAL SALES (USD Million)

U.S. Medicaid

0

Annual Reports

0

EXCIPIENTS
PATENTS & EXCLUSIVITIES

USFDA Orange Book Patents

0

USFDA Exclusivities

0

DIGITAL CONTENT

Blog #PharmaFlow

0

News

REF STANDARD

EDQM

USP

JP

0

Other Listed Suppliers

SERVICES

0

Looking for 101831-37-2 / Diclazuril API manufacturers, exporters & distributors?

Diclazuril manufacturers, exporters & distributors 1

86

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

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

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

API | Excipient name

Diclazuril

Synonyms

101831-37-2, Clinacox, Vecoxan, Nuoqiu, 2-(4-chlorophenyl)-2-[2,6-dichloro-4-(3,5-dioxo-1,2,4-triazin-2-yl)phenyl]acetonitrile, 2-(4-chlorophenyl)-2-(2,6-dichloro-4-(3,5-dioxo-4,5-dihydro-1,2,4-triazin-2(3h)-yl)phenyl)acetonitrile

Cas Number

101831-37-2

Unique Ingredient Identifier (UNII)

K110K1B1VE

About Diclazuril

Diclazuril is a coccidiostat.

Diclazuril Manufacturers

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

Diclazuril Suppliers

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

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

Diclazuril USDMF

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

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

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

Diclazuril CEP

A Diclazuril CEP of the European Pharmacopoeia monograph is often referred to as a Diclazuril Certificate of Suitability (COS). The purpose of a Diclazuril CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Diclazuril EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Diclazuril to their clients by showing that a Diclazuril CEP has been issued for it. The manufacturer submits a Diclazuril CEP (COS) as part of the market authorization procedure, and it takes on the role of a Diclazuril CEP holder for the record. Additionally, the data presented in the Diclazuril CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Diclazuril DMF.

A Diclazuril CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Diclazuril CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of Diclazuril suppliers with CEP (COS) on PharmaCompass.

Diclazuril 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 Diclazuril as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Diclazuril GMP

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

Diclazuril CoA

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

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

Diclazuril may be tested according to a variety of international standards, such as European Pharmacopoeia (Diclazuril EP), Diclazuril JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Diclazuril 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.
Ask Us for Pharmaceutical Supplier and Partner
Ask Us, Find A Supplier / Partner
No Commissions, No Strings Attached, Get Connected for FREE

What are you looking for?

How can we help you?

The request can't be empty

Please read our Privacy Policy carefully

You must agree to the privacy policy

The name can't be empty
The company can't be empty.
The email can't be empty Please enter a valid email.
The mobile can't be empty
Post Enquiry
POST ENQUIRY