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  • CREAM;TOPICAL - EQ 85MG BASE/GM
  • FOR SOLUTION;TOPICAL - 5%

Looking for 13009-99-9 / Mafenide API manufacturers, exporters & distributors?

Mafenide manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Mafenide

Synonyms

13009-99-9, 4-(aminomethyl)benzenesulfonamide acetate, Mafenamide acetate, Mafenide (acetate), Benzenesulfonamide, 4-(aminomethyl)-, monoacetate, Acetic acid;4-(aminomethyl)benzenesulfonamide

Cas Number

13009-99-9

Unique Ingredient Identifier (UNII)

RQ6LP6Z0WY

About Mafenide

A sulfonamide that inhibits the enzyme CARBONIC ANHYDRASE and is used as a topical anti-bacterial agent, especially in burn therapy.

Mafenide Acetate Manufacturers

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

Mafenide Acetate Suppliers

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

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

Mafenide Acetate USDMF

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

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

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

Mafenide Acetate 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 Mafenide Acetate as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Mafenide Acetate GMP

Mafenide Acetate 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 Mafenide Acetate 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 Mafenide Acetate GMP manufacturer or Mafenide Acetate GMP API supplier for your needs.

Mafenide Acetate CoA

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

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

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