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DRUG PRODUCT COMPOSITIONS
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Data Compilation #PharmaFlow
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API SUPPLIERS
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USDMF
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Lifecare Labs has been developing innovative products in specialist areas of medicine.
About the Company : Lifecare Labs specializes in producing bulk drugs (APIs) and intermediates that adhere to the industry's stringent quality parameters. Its objective is to deliver excellence throug...
Trusted Partner for Innovative, Sustainable, and High-Quality API Development and Production.
About the Company : Alven Laboratories is a pharmaceutical company specializing in the development, scale-up, and production of original and generic Active Pharmaceutical Ingredients (APIs). With expe...
Jai Radhe Sales is your partner for all your sourcing needs.
About the Company : Jai Radhe Sales was founded in 1999 as an out-of-the-box distribution firm specializing in the global supply of high-quality pharmaceutical ingredients. The firm provides complete ...
Delivering Quality APIs, Drug Intermediates, and Specialty Chemicals to Over 50 Countries Across the Globe.
About the Company : Zeal MediPharma is a globally recognized Star One Export House, serving customers in over 50 countries for more than two decades. We specialize in sourcing and exporting high-quali...
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
About the Company : LGM Pharma is a global leader in sourcing hard-to-find APIs and intermediates for the pharmaceutical and biotech industries. LGM is also a full service CDMO providing formulation, ...
Deccan Nutraceuticals: A global leader in the integrated development, manufacturing, and marketing of pharmaceutical products.
About the Company : Deccan Nutraceuticals Pvt. Ltd. (DNPL) is a group company of Alkaloids Corporation (India), was founded in 2001 and operates from a 22,000 sq. m. facility in Pune (India). Their co...
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
About the Company : HRV Global is a leading global manufacturer, seller & exporter of a wide range of APIs, advanced intermediates, pellets, food grade chemicals, food additives & food ingredients. It...
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
About the Company : Tenatra International was established as a proprietorship firm in 1999. It got off to a very good start, supporting clients in the United States, Mexico and Europe. As business opp...
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
About the Company : Founded in 1935, TAPI Technology & API Services has a long-standing tradition of advancing health through innovation and dedication. Today, we proudly build upon this legacy, drivi...
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API Imports and Exports
INTERMEDIATE SUPPLIERS
PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
2,2,2-Trichloroethyl chloroformate
CAS Number : 17341-93-4
End Use API : Cabergoline
About The Company : PMC Isochem is a CDMO company acquired by PMC International in 2017. It manufactures cGMP intermediates, active pharmaceutical ingredients and functional excipi...
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Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info :
Registration Country : India
Brand Name : Cabergoline
Dosage Form : Tablet
Dosage Strength : 0.5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
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Evonik
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REF. STANDARDS & IMPURITIES
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PharmaCompass offers a list of Cabergoline 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 Cabergoline manufacturer or Cabergoline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cabergoline manufacturer or Cabergoline supplier.
PharmaCompass also assists you with knowing the Cabergoline API Price utilized in the formulation of products. Cabergoline API Price is not always fixed or binding as the Cabergoline Price is obtained through a variety of data sources. The Cabergoline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cabaseril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cabaseril, including repackagers and relabelers. The FDA regulates Cabaseril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cabaseril 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 Cabaseril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cabaseril supplier is an individual or a company that provides Cabaseril active pharmaceutical ingredient (API) or Cabaseril finished formulations upon request. The Cabaseril suppliers may include Cabaseril API manufacturers, exporters, distributors and traders.
click here to find a list of Cabaseril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cabaseril DMF (Drug Master File) is a document detailing the whole manufacturing process of Cabaseril active pharmaceutical ingredient (API) in detail. Different forms of Cabaseril DMFs exist exist since differing nations have different regulations, such as Cabaseril USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cabaseril DMF submitted to regulatory agencies in the US is known as a USDMF. Cabaseril USDMF includes data on Cabaseril's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cabaseril USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cabaseril suppliers with USDMF on PharmaCompass.
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 Cabaseril Drug Master File in Japan (Cabaseril JDMF) empowers Cabaseril 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 Cabaseril JDMF during the approval evaluation for pharmaceutical products. At the time of Cabaseril 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 Cabaseril suppliers with JDMF 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 Cabaseril Drug Master File in Korea (Cabaseril KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cabaseril. The MFDS reviews the Cabaseril KDMF as part of the drug registration process and uses the information provided in the Cabaseril KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cabaseril 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 Cabaseril API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cabaseril suppliers with KDMF on PharmaCompass.
A Cabaseril CEP of the European Pharmacopoeia monograph is often referred to as a Cabaseril Certificate of Suitability (COS). The purpose of a Cabaseril CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cabaseril EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cabaseril to their clients by showing that a Cabaseril CEP has been issued for it. The manufacturer submits a Cabaseril CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cabaseril CEP holder for the record. Additionally, the data presented in the Cabaseril CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cabaseril DMF.
A Cabaseril CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cabaseril 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 Cabaseril suppliers with CEP (COS) on PharmaCompass.
A Cabaseril written confirmation (Cabaseril WC) is an official document issued by a regulatory agency to a Cabaseril manufacturer, verifying that the manufacturing facility of a Cabaseril active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Cabaseril APIs or Cabaseril finished pharmaceutical products to another nation, regulatory agencies frequently require a Cabaseril WC (written confirmation) as part of the regulatory process.
click here to find a list of Cabaseril 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 Cabaseril as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cabaseril 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 Cabaseril 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 Cabaseril and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cabaseril NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cabaseril suppliers with NDC on PharmaCompass.
Cabaseril 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 Cabaseril 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 Cabaseril GMP manufacturer or Cabaseril GMP API supplier for your needs.
A Cabaseril CoA (Certificate of Analysis) is a formal document that attests to Cabaseril's compliance with Cabaseril specifications and serves as a tool for batch-level quality control.
Cabaseril CoA mostly includes findings from lab analyses of a specific batch. For each Cabaseril 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.
Cabaseril may be tested according to a variety of international standards, such as European Pharmacopoeia (Cabaseril EP), Cabaseril JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cabaseril USP).
