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Looking for 75-47-8 / Iodoform API manufacturers, exporters & distributors?

Iodoform manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Iodoform

Synonyms

Triiodomethane, 75-47-8, Methane, triiodo-, Carbon triiodide, Jodoform, Chi3

Cas Number

75-47-8

Unique Ingredient Identifier (UNII)

KXI2J76489

About Iodoform

iodoform is a natural product found in Asparagopsis taxiformis with data available.

MolPort-001-783-761 Manufacturers

A MolPort-001-783-761 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-783-761, including repackagers and relabelers. The FDA regulates MolPort-001-783-761 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-783-761 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 MolPort-001-783-761 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-001-783-761 Suppliers

A MolPort-001-783-761 supplier is an individual or a company that provides MolPort-001-783-761 active pharmaceutical ingredient (API) or MolPort-001-783-761 finished formulations upon request. The MolPort-001-783-761 suppliers may include MolPort-001-783-761 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-001-783-761 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-001-783-761 USDMF

A MolPort-001-783-761 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-783-761 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-783-761 DMFs exist exist since differing nations have different regulations, such as MolPort-001-783-761 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A MolPort-001-783-761 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-783-761 USDMF includes data on MolPort-001-783-761's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-783-761 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of MolPort-001-783-761 suppliers with USDMF on PharmaCompass.

MolPort-001-783-761 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 MolPort-001-783-761 Drug Master File in Japan (MolPort-001-783-761 JDMF) empowers MolPort-001-783-761 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 MolPort-001-783-761 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-001-783-761 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 MolPort-001-783-761 suppliers with JDMF on PharmaCompass.

MolPort-001-783-761 WC

A MolPort-001-783-761 written confirmation (MolPort-001-783-761 WC) is an official document issued by a regulatory agency to a MolPort-001-783-761 manufacturer, verifying that the manufacturing facility of a MolPort-001-783-761 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting MolPort-001-783-761 APIs or MolPort-001-783-761 finished pharmaceutical products to another nation, regulatory agencies frequently require a MolPort-001-783-761 WC (written confirmation) as part of the regulatory process.

click here to find a list of MolPort-001-783-761 suppliers with Written Confirmation (WC) on PharmaCompass.

MolPort-001-783-761 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 MolPort-001-783-761 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for MolPort-001-783-761 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 MolPort-001-783-761 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 MolPort-001-783-761 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MolPort-001-783-761 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of MolPort-001-783-761 suppliers with NDC on PharmaCompass.

MolPort-001-783-761 GMP

MolPort-001-783-761 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 MolPort-001-783-761 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 MolPort-001-783-761 GMP manufacturer or MolPort-001-783-761 GMP API supplier for your needs.

MolPort-001-783-761 CoA

A MolPort-001-783-761 CoA (Certificate of Analysis) is a formal document that attests to MolPort-001-783-761's compliance with MolPort-001-783-761 specifications and serves as a tool for batch-level quality control.

MolPort-001-783-761 CoA mostly includes findings from lab analyses of a specific batch. For each MolPort-001-783-761 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.

MolPort-001-783-761 may be tested according to a variety of international standards, such as European Pharmacopoeia (MolPort-001-783-761 EP), MolPort-001-783-761 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MolPort-001-783-761 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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