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Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
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Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
Isonipecotic acid/4-Piperidinecarboxylic acid
CAS Number : 498-94-2
End Use API : Lasmiditan
About The Company : Tagoor Laboratories, established in 2018, is a part of the Tagoor Group. It specializes in providing APIs, advanced intermediates and key starting materials for...
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ABOUT THIS PAGE
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PharmaCompass offers a list of Lasmiditan 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 Lasmiditan manufacturer or Lasmiditan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lasmiditan manufacturer or Lasmiditan supplier.
PharmaCompass also assists you with knowing the Lasmiditan API Price utilized in the formulation of products. Lasmiditan API Price is not always fixed or binding as the Lasmiditan Price is obtained through a variety of data sources. The Lasmiditan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lasmiditan hemisuccinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lasmiditan hemisuccinate, including repackagers and relabelers. The FDA regulates Lasmiditan hemisuccinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lasmiditan hemisuccinate 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 Lasmiditan hemisuccinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lasmiditan hemisuccinate supplier is an individual or a company that provides Lasmiditan hemisuccinate active pharmaceutical ingredient (API) or Lasmiditan hemisuccinate finished formulations upon request. The Lasmiditan hemisuccinate suppliers may include Lasmiditan hemisuccinate API manufacturers, exporters, distributors and traders.
click here to find a list of Lasmiditan hemisuccinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lasmiditan hemisuccinate DMF (Drug Master File) is a document detailing the whole manufacturing process of Lasmiditan hemisuccinate active pharmaceutical ingredient (API) in detail. Different forms of Lasmiditan hemisuccinate DMFs exist exist since differing nations have different regulations, such as Lasmiditan hemisuccinate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lasmiditan hemisuccinate DMF submitted to regulatory agencies in the US is known as a USDMF. Lasmiditan hemisuccinate USDMF includes data on Lasmiditan hemisuccinate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lasmiditan hemisuccinate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lasmiditan hemisuccinate 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 Lasmiditan hemisuccinate Drug Master File in Korea (Lasmiditan hemisuccinate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Lasmiditan hemisuccinate. The MFDS reviews the Lasmiditan hemisuccinate KDMF as part of the drug registration process and uses the information provided in the Lasmiditan hemisuccinate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Lasmiditan hemisuccinate 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 Lasmiditan hemisuccinate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Lasmiditan hemisuccinate suppliers with KDMF 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 Lasmiditan hemisuccinate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lasmiditan hemisuccinate 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 Lasmiditan hemisuccinate 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 Lasmiditan hemisuccinate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lasmiditan hemisuccinate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Lasmiditan hemisuccinate suppliers with NDC on PharmaCompass.
Lasmiditan hemisuccinate 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 Lasmiditan hemisuccinate 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 Lasmiditan hemisuccinate GMP manufacturer or Lasmiditan hemisuccinate GMP API supplier for your needs.
A Lasmiditan hemisuccinate CoA (Certificate of Analysis) is a formal document that attests to Lasmiditan hemisuccinate's compliance with Lasmiditan hemisuccinate specifications and serves as a tool for batch-level quality control.
Lasmiditan hemisuccinate CoA mostly includes findings from lab analyses of a specific batch. For each Lasmiditan hemisuccinate 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.
Lasmiditan hemisuccinate may be tested according to a variety of international standards, such as European Pharmacopoeia (Lasmiditan hemisuccinate EP), Lasmiditan hemisuccinate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lasmiditan hemisuccinate USP).
