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Looking for 64-17-5 / Ethanol API manufacturers, exporters & distributors?

Ethanol manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Ethanol

Synonyms

Ethyl alcohol, Alcohol, 64-17-5, Grain alcohol, Methylcarbinol, Ethyl hydroxide

Cas Number

64-17-5

Unique Ingredient Identifier (UNII)

3K9958V90M

About Ethanol

A clear, colorless liquid rapidly absorbed from the gastrointestinal tract and distributed throughout the body. It has bactericidal activity and is used often as a topical disinfectant. It is widely used as a solvent and preservative in pharmaceutical preparations as well as serving as the primary ingredient in ALCOHOLIC BEVERAGES.

02877_FLUKA Manufacturers

A 02877_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 02877_FLUKA, including repackagers and relabelers. The FDA regulates 02877_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 02877_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 02877_FLUKA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

02877_FLUKA Suppliers

A 02877_FLUKA supplier is an individual or a company that provides 02877_FLUKA active pharmaceutical ingredient (API) or 02877_FLUKA finished formulations upon request. The 02877_FLUKA suppliers may include 02877_FLUKA API manufacturers, exporters, distributors and traders.

click here to find a list of 02877_FLUKA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

02877_FLUKA USDMF

A 02877_FLUKA DMF (Drug Master File) is a document detailing the whole manufacturing process of 02877_FLUKA active pharmaceutical ingredient (API) in detail. Different forms of 02877_FLUKA DMFs exist exist since differing nations have different regulations, such as 02877_FLUKA USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 02877_FLUKA DMF submitted to regulatory agencies in the US is known as a USDMF. 02877_FLUKA USDMF includes data on 02877_FLUKA's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 02877_FLUKA USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 02877_FLUKA suppliers with USDMF on PharmaCompass.

02877_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 02877_FLUKA Drug Master File in Japan (02877_FLUKA JDMF) empowers 02877_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 02877_FLUKA JDMF during the approval evaluation for pharmaceutical products. At the time of 02877_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 02877_FLUKA suppliers with JDMF on PharmaCompass.

02877_FLUKA KDMF

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

Pharmaceutical companies submit a 02877_FLUKA Drug Master File in Korea (02877_FLUKA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 02877_FLUKA. The MFDS reviews the 02877_FLUKA KDMF as part of the drug registration process and uses the information provided in the 02877_FLUKA KDMF to evaluate the safety and efficacy of the drug.

After submitting a 02877_FLUKA 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 02877_FLUKA API can apply through the Korea Drug Master File (KDMF).

click here to find a list of 02877_FLUKA suppliers with KDMF on PharmaCompass.

02877_FLUKA CEP

A 02877_FLUKA CEP of the European Pharmacopoeia monograph is often referred to as a 02877_FLUKA Certificate of Suitability (COS). The purpose of a 02877_FLUKA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 02877_FLUKA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 02877_FLUKA to their clients by showing that a 02877_FLUKA CEP has been issued for it. The manufacturer submits a 02877_FLUKA CEP (COS) as part of the market authorization procedure, and it takes on the role of a 02877_FLUKA CEP holder for the record. Additionally, the data presented in the 02877_FLUKA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 02877_FLUKA DMF.

A 02877_FLUKA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 02877_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 02877_FLUKA suppliers with CEP (COS) on PharmaCompass.

02877_FLUKA GMP

02877_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 02877_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 02877_FLUKA GMP manufacturer or 02877_FLUKA GMP API supplier for your needs.

02877_FLUKA CoA

A 02877_FLUKA CoA (Certificate of Analysis) is a formal document that attests to 02877_FLUKA's compliance with 02877_FLUKA specifications and serves as a tool for batch-level quality control.

02877_FLUKA CoA mostly includes findings from lab analyses of a specific batch. For each 02877_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.

02877_FLUKA may be tested according to a variety of international standards, such as European Pharmacopoeia (02877_FLUKA EP), 02877_FLUKA JP (Japanese Pharmacopeia) and the US Pharmacopoeia (02877_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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