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Looking for 53164-05-9 / Acemetacin API manufacturers, exporters & distributors?

Acemetacin manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Acemetacin

Synonyms

53164-05-9, Rantudil, Emflex, Acemix, Acemetacinum, Acemetacina

Cas Number

53164-05-9

Unique Ingredient Identifier (UNII)

5V141XK28X

About Acemetacin

Acemetacin is a carboxymethyl ester of indometacin. It is a potent non-steroidal anti-inflammatory drug, derived from the indol-3-acetic acid, whose activity is thought to be mainly through its active metabolite indomethacin. In clinical trials, acemetacin exhibits a better gastric tolerability compared to its active metabolite indometacin. It was developed by E. Merck and Company in Germany as an attempt to provide a safer drug but other than the amelioration on the gastrointestinal effects, the metabolism of acetamicin led to the formation of indomethacin and it kept the same side effects.

MolPort-002-045-405 Manufacturers

A MolPort-002-045-405 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-002-045-405, including repackagers and relabelers. The FDA regulates MolPort-002-045-405 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-002-045-405 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-002-045-405 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-002-045-405 Suppliers

A MolPort-002-045-405 supplier is an individual or a company that provides MolPort-002-045-405 active pharmaceutical ingredient (API) or MolPort-002-045-405 finished formulations upon request. The MolPort-002-045-405 suppliers may include MolPort-002-045-405 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-002-045-405 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-002-045-405 USDMF

A MolPort-002-045-405 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-002-045-405 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-002-045-405 DMFs exist exist since differing nations have different regulations, such as MolPort-002-045-405 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A MolPort-002-045-405 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-002-045-405 USDMF includes data on MolPort-002-045-405's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-002-045-405 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of MolPort-002-045-405 suppliers with USDMF on PharmaCompass.

MolPort-002-045-405 CEP

A MolPort-002-045-405 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-002-045-405 Certificate of Suitability (COS). The purpose of a MolPort-002-045-405 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-002-045-405 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-002-045-405 to their clients by showing that a MolPort-002-045-405 CEP has been issued for it. The manufacturer submits a MolPort-002-045-405 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-002-045-405 CEP holder for the record. Additionally, the data presented in the MolPort-002-045-405 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-002-045-405 DMF.

A MolPort-002-045-405 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-002-045-405 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 MolPort-002-045-405 suppliers with CEP (COS) on PharmaCompass.

MolPort-002-045-405 WC

A MolPort-002-045-405 written confirmation (MolPort-002-045-405 WC) is an official document issued by a regulatory agency to a MolPort-002-045-405 manufacturer, verifying that the manufacturing facility of a MolPort-002-045-405 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting MolPort-002-045-405 APIs or MolPort-002-045-405 finished pharmaceutical products to another nation, regulatory agencies frequently require a MolPort-002-045-405 WC (written confirmation) as part of the regulatory process.

click here to find a list of MolPort-002-045-405 suppliers with Written Confirmation (WC) on PharmaCompass.

MolPort-002-045-405 GMP

MolPort-002-045-405 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-002-045-405 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-002-045-405 GMP manufacturer or MolPort-002-045-405 GMP API supplier for your needs.

MolPort-002-045-405 CoA

A MolPort-002-045-405 CoA (Certificate of Analysis) is a formal document that attests to MolPort-002-045-405's compliance with MolPort-002-045-405 specifications and serves as a tool for batch-level quality control.

MolPort-002-045-405 CoA mostly includes findings from lab analyses of a specific batch. For each MolPort-002-045-405 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-002-045-405 may be tested according to a variety of international standards, such as European Pharmacopoeia (MolPort-002-045-405 EP), MolPort-002-045-405 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MolPort-002-045-405 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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