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PharmaCompass offers a list of Atomoxetin Hydrochloride 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 Atomoxetin Hydrochloride manufacturer or Atomoxetin Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Atomoxetin Hydrochloride manufacturer or Atomoxetin Hydrochloride supplier.
PharmaCompass also assists you with knowing the Atomoxetin Hydrochloride API Price utilized in the formulation of products. Atomoxetin Hydrochloride API Price is not always fixed or binding as the Atomoxetin Hydrochloride Price is obtained through a variety of data sources. The Atomoxetin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Atomoxetine HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Atomoxetine HCl, including repackagers and relabelers. The FDA regulates Atomoxetine HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Atomoxetine HCl 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 Atomoxetine HCl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Atomoxetine HCl supplier is an individual or a company that provides Atomoxetine HCl active pharmaceutical ingredient (API) or Atomoxetine HCl finished formulations upon request. The Atomoxetine HCl suppliers may include Atomoxetine HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Atomoxetine HCl suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Atomoxetine HCl DMF (Drug Master File) is a document detailing the whole manufacturing process of Atomoxetine HCl active pharmaceutical ingredient (API) in detail. Different forms of Atomoxetine HCl DMFs exist exist since differing nations have different regulations, such as Atomoxetine HCl USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Atomoxetine HCl DMF submitted to regulatory agencies in the US is known as a USDMF. Atomoxetine HCl USDMF includes data on Atomoxetine HCl's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Atomoxetine HCl USDMF is kept confidential to protect the manufacturer’s intellectual property.
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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 Atomoxetine HCl Drug Master File in Japan (Atomoxetine HCl JDMF) empowers Atomoxetine HCl 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 Atomoxetine HCl JDMF during the approval evaluation for pharmaceutical products. At the time of Atomoxetine HCl JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Atomoxetine HCl Drug Master File in Korea (Atomoxetine HCl KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Atomoxetine HCl. The MFDS reviews the Atomoxetine HCl KDMF as part of the drug registration process and uses the information provided in the Atomoxetine HCl KDMF to evaluate the safety and efficacy of the drug.
After submitting a Atomoxetine HCl 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 Atomoxetine HCl API can apply through the Korea Drug Master File (KDMF).
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A Atomoxetine HCl CEP of the European Pharmacopoeia monograph is often referred to as a Atomoxetine HCl Certificate of Suitability (COS). The purpose of a Atomoxetine HCl CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Atomoxetine HCl EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Atomoxetine HCl to their clients by showing that a Atomoxetine HCl CEP has been issued for it. The manufacturer submits a Atomoxetine HCl CEP (COS) as part of the market authorization procedure, and it takes on the role of a Atomoxetine HCl CEP holder for the record. Additionally, the data presented in the Atomoxetine HCl CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Atomoxetine HCl DMF.
A Atomoxetine HCl CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Atomoxetine HCl 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 Atomoxetine HCl suppliers with CEP (COS) on PharmaCompass.
A Atomoxetine HCl written confirmation (Atomoxetine HCl WC) is an official document issued by a regulatory agency to a Atomoxetine HCl manufacturer, verifying that the manufacturing facility of a Atomoxetine HCl active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Atomoxetine HCl APIs or Atomoxetine HCl finished pharmaceutical products to another nation, regulatory agencies frequently require a Atomoxetine HCl WC (written confirmation) as part of the regulatory process.
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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 Atomoxetine HCl as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Atomoxetine HCl API and other APIs are published in this directory by the FDA.
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 Atomoxetine HCl 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.
The NDC directory also contains data on finished compounded human drug products that contain Atomoxetine HCl and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Atomoxetine HCl NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Atomoxetine HCl suppliers with NDC on PharmaCompass.
Atomoxetine HCl 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 Atomoxetine HCl 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 Atomoxetine HCl GMP manufacturer or Atomoxetine HCl GMP API supplier for your needs.
A Atomoxetine HCl CoA (Certificate of Analysis) is a formal document that attests to Atomoxetine HCl's compliance with Atomoxetine HCl specifications and serves as a tool for batch-level quality control.
Atomoxetine HCl CoA mostly includes findings from lab analyses of a specific batch. For each Atomoxetine HCl 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.
Atomoxetine HCl may be tested according to a variety of international standards, such as European Pharmacopoeia (Atomoxetine HCl EP), Atomoxetine HCl JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Atomoxetine HCl USP).
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