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LEBSA- Your strategic API source for niche molecules.
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LEBSA- Your strategic API source for niche molecules.
Registrant Name : Wonpung Pharmaceutical Co., Ltd.
Registration Date : 2023-09-20
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Manufacturer Address : Ctra. De L'Hospitalet, 34 08940 Cornellà Barcelona, Spain
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LEBSA- Your strategic API source for niche molecules.
About the Company : Lebsa is an innovative European laboratory that specializes in the synthesis, manufacture and commercialization of APIs with a focus on niche products. With a track record spanning...
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PharmaCompass offers a list of Octenidine 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 Octenidine Hydrochloride manufacturer or Octenidine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Octenidine Hydrochloride manufacturer or Octenidine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Octenidine Hydrochloride API Price utilized in the formulation of products. Octenidine Hydrochloride API Price is not always fixed or binding as the Octenidine Hydrochloride Price is obtained through a variety of data sources. The Octenidine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Octenidine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Octenidine Hydrochloride, including repackagers and relabelers. The FDA regulates Octenidine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Octenidine Hydrochloride 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 Octenidine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Octenidine Hydrochloride supplier is an individual or a company that provides Octenidine Hydrochloride active pharmaceutical ingredient (API) or Octenidine Hydrochloride finished formulations upon request. The Octenidine Hydrochloride suppliers may include Octenidine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Octenidine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Octenidine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Octenidine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Octenidine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Octenidine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Octenidine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Octenidine Hydrochloride USDMF includes data on Octenidine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Octenidine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Octenidine Hydrochloride suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Octenidine Hydrochloride Drug Master File in Korea (Octenidine Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Octenidine Hydrochloride. The MFDS reviews the Octenidine Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Octenidine Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Octenidine Hydrochloride 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 Octenidine Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Octenidine Hydrochloride suppliers with KDMF on PharmaCompass.
A Octenidine Hydrochloride written confirmation (Octenidine Hydrochloride WC) is an official document issued by a regulatory agency to a Octenidine Hydrochloride manufacturer, verifying that the manufacturing facility of a Octenidine Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Octenidine Hydrochloride APIs or Octenidine Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Octenidine Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Octenidine Hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
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 Octenidine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Octenidine Hydrochloride 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 Octenidine Hydrochloride 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 Octenidine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Octenidine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Octenidine Hydrochloride suppliers with NDC on PharmaCompass.
Octenidine Hydrochloride 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 Octenidine Hydrochloride 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 Octenidine Hydrochloride GMP manufacturer or Octenidine Hydrochloride GMP API supplier for your needs.
A Octenidine Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Octenidine Hydrochloride's compliance with Octenidine Hydrochloride specifications and serves as a tool for batch-level quality control.
Octenidine Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Octenidine Hydrochloride 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.
Octenidine Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Octenidine Hydrochloride EP), Octenidine Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Octenidine Hydrochloride USP).
