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Looking for 94-09-7 / Benzocaine API manufacturers, exporters & distributors?

Benzocaine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Benzocaine

Synonyms

Ethyl 4-aminobenzoate, 94-09-7, Ethyl aminobenzoate, Ethyl p-aminobenzoate, Americaine, Anaesthesin

Cas Number

94-09-7

Unique Ingredient Identifier (UNII)

U3RSY48JW5

About Benzocaine

A surface anesthetic that acts by preventing transmission of impulses along nerve fibers and at nerve endings.

06952_FLUKA Manufacturers

A 06952_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 06952_FLUKA, including repackagers and relabelers. The FDA regulates 06952_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 06952_FLUKA 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 06952_FLUKA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

06952_FLUKA Suppliers

A 06952_FLUKA supplier is an individual or a company that provides 06952_FLUKA active pharmaceutical ingredient (API) or 06952_FLUKA finished formulations upon request. The 06952_FLUKA suppliers may include 06952_FLUKA API manufacturers, exporters, distributors and traders.

click here to find a list of 06952_FLUKA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

06952_FLUKA USDMF

A 06952_FLUKA DMF (Drug Master File) is a document detailing the whole manufacturing process of 06952_FLUKA active pharmaceutical ingredient (API) in detail. Different forms of 06952_FLUKA DMFs exist exist since differing nations have different regulations, such as 06952_FLUKA USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 06952_FLUKA DMF submitted to regulatory agencies in the US is known as a USDMF. 06952_FLUKA USDMF includes data on 06952_FLUKA's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 06952_FLUKA USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 06952_FLUKA suppliers with USDMF on PharmaCompass.

06952_FLUKA 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 06952_FLUKA Drug Master File in Japan (06952_FLUKA JDMF) empowers 06952_FLUKA 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 06952_FLUKA JDMF during the approval evaluation for pharmaceutical products. At the time of 06952_FLUKA 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 06952_FLUKA suppliers with JDMF on PharmaCompass.

06952_FLUKA CEP

A 06952_FLUKA CEP of the European Pharmacopoeia monograph is often referred to as a 06952_FLUKA Certificate of Suitability (COS). The purpose of a 06952_FLUKA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 06952_FLUKA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 06952_FLUKA to their clients by showing that a 06952_FLUKA CEP has been issued for it. The manufacturer submits a 06952_FLUKA CEP (COS) as part of the market authorization procedure, and it takes on the role of a 06952_FLUKA CEP holder for the record. Additionally, the data presented in the 06952_FLUKA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 06952_FLUKA DMF.

A 06952_FLUKA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 06952_FLUKA 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 06952_FLUKA suppliers with CEP (COS) on PharmaCompass.

06952_FLUKA WC

A 06952_FLUKA written confirmation (06952_FLUKA WC) is an official document issued by a regulatory agency to a 06952_FLUKA manufacturer, verifying that the manufacturing facility of a 06952_FLUKA active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 06952_FLUKA APIs or 06952_FLUKA finished pharmaceutical products to another nation, regulatory agencies frequently require a 06952_FLUKA WC (written confirmation) as part of the regulatory process.

click here to find a list of 06952_FLUKA suppliers with Written Confirmation (WC) on PharmaCompass.

06952_FLUKA 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 06952_FLUKA as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for 06952_FLUKA 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 06952_FLUKA 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 06952_FLUKA and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 06952_FLUKA NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of 06952_FLUKA suppliers with NDC on PharmaCompass.

06952_FLUKA GMP

06952_FLUKA 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 06952_FLUKA 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 06952_FLUKA GMP manufacturer or 06952_FLUKA GMP API supplier for your needs.

06952_FLUKA CoA

A 06952_FLUKA CoA (Certificate of Analysis) is a formal document that attests to 06952_FLUKA's compliance with 06952_FLUKA specifications and serves as a tool for batch-level quality control.

06952_FLUKA CoA mostly includes findings from lab analyses of a specific batch. For each 06952_FLUKA 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.

06952_FLUKA may be tested according to a variety of international standards, such as European Pharmacopoeia (06952_FLUKA EP), 06952_FLUKA JP (Japanese Pharmacopeia) and the US Pharmacopoeia (06952_FLUKA 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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