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Looking for 41575-94-4 / Carboplatin API manufacturers, exporters & distributors?

Carboplatin manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Carboplatin

Synonyms

Paraplatin, Cbdca, Jm-8, Cis-diammine(1,1-cyclobutanedicarboxylato)platinum, Nsc 241240, Nsc-241240

Cas Number

41575-94-4

Unique Ingredient Identifier (UNII)

BG3F62OND5

About Carboplatin

An organoplatinum compound that possesses antineoplastic activity.

1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM Manufacturers

A 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM, including repackagers and relabelers. The FDA regulates 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM 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 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM Suppliers

A 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM supplier is an individual or a company that provides 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM active pharmaceutical ingredient (API) or 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM finished formulations upon request. The 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM suppliers may include 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM API manufacturers, exporters, distributors and traders.

click here to find a list of 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM USDMF

A 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM DMF (Drug Master File) is a document detailing the whole manufacturing process of 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM active pharmaceutical ingredient (API) in detail. Different forms of 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM DMFs exist exist since differing nations have different regulations, such as 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM DMF submitted to regulatory agencies in the US is known as a USDMF. 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM USDMF includes data on 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM suppliers with USDMF on PharmaCompass.

1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM 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 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM Drug Master File in Japan (1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM JDMF) empowers 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM 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 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM JDMF during the approval evaluation for pharmaceutical products. At the time of 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM 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 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM suppliers with JDMF on PharmaCompass.

1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM KDMF

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

Pharmaceutical companies submit a 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM Drug Master File in Korea (1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM. The MFDS reviews the 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM KDMF as part of the drug registration process and uses the information provided in the 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM KDMF to evaluate the safety and efficacy of the drug.

After submitting a 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM 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 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM API can apply through the Korea Drug Master File (KDMF).

click here to find a list of 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM suppliers with KDMF on PharmaCompass.

1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM CEP

A 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM CEP of the European Pharmacopoeia monograph is often referred to as a 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM Certificate of Suitability (COS). The purpose of a 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM to their clients by showing that a 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM CEP has been issued for it. The manufacturer submits a 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM CEP (COS) as part of the market authorization procedure, and it takes on the role of a 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM CEP holder for the record. Additionally, the data presented in the 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM DMF.

A 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM 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 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM suppliers with CEP (COS) on PharmaCompass.

1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM WC

A 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM written confirmation (1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM WC) is an official document issued by a regulatory agency to a 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM manufacturer, verifying that the manufacturing facility of a 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM APIs or 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM finished pharmaceutical products to another nation, regulatory agencies frequently require a 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM WC (written confirmation) as part of the regulatory process.

click here to find a list of 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM suppliers with Written Confirmation (WC) on PharmaCompass.

1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM 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 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM 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 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM 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 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM suppliers with NDC on PharmaCompass.

1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM GMP

1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM 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 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM 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 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM GMP manufacturer or 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM GMP API supplier for your needs.

1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM CoA

A 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM CoA (Certificate of Analysis) is a formal document that attests to 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM's compliance with 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM specifications and serves as a tool for batch-level quality control.

1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM CoA mostly includes findings from lab analyses of a specific batch. For each 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM 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.

1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM may be tested according to a variety of international standards, such as European Pharmacopoeia (1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM EP), 1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1,1-CYCLOBUTANEDICARBOXYLATODIAMMINE PLATINUM 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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