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Looking for 305-03-3 / Chlorambucil API manufacturers, exporters & distributors?

Chlorambucil manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Chlorambucil

Synonyms

305-03-3, Ambochlorin, Leukeran, Chloroambucil, Chloraminophen, Chlorbutin

Cas Number

305-03-3

Unique Ingredient Identifier (UNII)

18D0SL7309

About Chlorambucil

A nitrogen mustard alkylating agent used as antineoplastic for chronic lymphocytic leukemia, Hodgkin's disease, and others. Although it is less toxic than most other nitrogen mustards, it has been listed as a known carcinogen in the Fourth Annual Report on Carcinogens (NTP 85-002, 1985). (Merck Index, 11th ed)

Prestwick3_001079 Manufacturers

A Prestwick3_001079 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_001079, including repackagers and relabelers. The FDA regulates Prestwick3_001079 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_001079 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 Prestwick3_001079 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Prestwick3_001079 Suppliers

A Prestwick3_001079 supplier is an individual or a company that provides Prestwick3_001079 active pharmaceutical ingredient (API) or Prestwick3_001079 finished formulations upon request. The Prestwick3_001079 suppliers may include Prestwick3_001079 API manufacturers, exporters, distributors and traders.

click here to find a list of Prestwick3_001079 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Prestwick3_001079 USDMF

A Prestwick3_001079 DMF (Drug Master File) is a document detailing the whole manufacturing process of Prestwick3_001079 active pharmaceutical ingredient (API) in detail. Different forms of Prestwick3_001079 DMFs exist exist since differing nations have different regulations, such as Prestwick3_001079 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Prestwick3_001079 DMF submitted to regulatory agencies in the US is known as a USDMF. Prestwick3_001079 USDMF includes data on Prestwick3_001079's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Prestwick3_001079 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Prestwick3_001079 suppliers with USDMF on PharmaCompass.

Prestwick3_001079 CEP

A Prestwick3_001079 CEP of the European Pharmacopoeia monograph is often referred to as a Prestwick3_001079 Certificate of Suitability (COS). The purpose of a Prestwick3_001079 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Prestwick3_001079 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Prestwick3_001079 to their clients by showing that a Prestwick3_001079 CEP has been issued for it. The manufacturer submits a Prestwick3_001079 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Prestwick3_001079 CEP holder for the record. Additionally, the data presented in the Prestwick3_001079 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Prestwick3_001079 DMF.

A Prestwick3_001079 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Prestwick3_001079 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 Prestwick3_001079 suppliers with CEP (COS) on PharmaCompass.

Prestwick3_001079 WC

A Prestwick3_001079 written confirmation (Prestwick3_001079 WC) is an official document issued by a regulatory agency to a Prestwick3_001079 manufacturer, verifying that the manufacturing facility of a Prestwick3_001079 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Prestwick3_001079 APIs or Prestwick3_001079 finished pharmaceutical products to another nation, regulatory agencies frequently require a Prestwick3_001079 WC (written confirmation) as part of the regulatory process.

click here to find a list of Prestwick3_001079 suppliers with Written Confirmation (WC) on PharmaCompass.

Prestwick3_001079 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 Prestwick3_001079 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Prestwick3_001079 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 Prestwick3_001079 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 Prestwick3_001079 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Prestwick3_001079 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Prestwick3_001079 suppliers with NDC on PharmaCompass.

Prestwick3_001079 GMP

Prestwick3_001079 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 Prestwick3_001079 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 Prestwick3_001079 GMP manufacturer or Prestwick3_001079 GMP API supplier for your needs.

Prestwick3_001079 CoA

A Prestwick3_001079 CoA (Certificate of Analysis) is a formal document that attests to Prestwick3_001079's compliance with Prestwick3_001079 specifications and serves as a tool for batch-level quality control.

Prestwick3_001079 CoA mostly includes findings from lab analyses of a specific batch. For each Prestwick3_001079 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.

Prestwick3_001079 may be tested according to a variety of international standards, such as European Pharmacopoeia (Prestwick3_001079 EP), Prestwick3_001079 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Prestwick3_001079 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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