Synopsis
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USDMF
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JDMF
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NDC API
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VMF
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FDA Orange Book
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Canada
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Australia
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South Africa
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
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FDF
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
API SUPPLIERS
Cosma S.p.A., part of CFM Group with AMSA & Clarochem, provides global pharma & veterinary health with 300+ tons of FDA-approved APIs.
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
EU-WC
KDMF
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
Lewens Labs transforms healthcare with innovative, sustainable, and affordable pharmaceutical solutions worldwide.
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
CEP/COS
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Certificate Number : CEP 2023-110 - Rev 00
Status : Valid
Issue Date : 2024-05-24
Type : Chemical
Substance Number : 1535
Certificate Number : R1-CEP 2012-083 - Rev 01
Status : Valid
Issue Date : 2020-01-17
Type : Chemical
Substance Number : 1535
Certificate Number : R1-CEP 2013-121 - Rev 00
Status : Valid
Issue Date : 2020-03-31
Type : Chemical
Substance Number : 1535
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results] EU WC
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Date of Issue : 2025-07-24
Valid Till : 2028-07-21
Written Confirmation Number : WC-0150N
Address of the Firm : API Unit-l, R.S. No. 50/1, Mukteswarapuram Village,\r\nJaggaiahpet Mandal, NTR D...
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]KDMF
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Registrant Name : Iksoo Pharmaceutical Co., Ltd.
Registration Date : 2025-06-23
Registration Number : 20250623-137-H-447-14
Manufacturer Name : Cohance Lifesciences Limited
Manufacturer Address : API Unit-I, RS 50/1, Mukteswarapuram Village, Jaggaiahpet Mandal, NTR District – 52...
Registrant Name : Pharmaking Co., Ltd.
Registration Date : 2015-05-22
Registration Number : 20131029-137-H-241-10(2)
Manufacturer Name : Clarochem Ireland Ltd.
Manufacturer Address : Damastown, Mulhuddart, Dublin 15, Ireland
Registrant Name : Goodwills Co., Ltd.
Registration Date : 2013-10-29
Registration Number : 20131029-137-H-241-10
Manufacturer Name : Clarochem Ireland Ltd.
Manufacturer Address : Damastown, Mulhuddart, Dublin 15, Ireland
Registrant Name : Sampoong Finechem Co., Ltd.
Registration Date : 2022-11-15
Registration Number : 20131029-137-H-241-10(4)
Manufacturer Name : Clarochem Ireland Ltd.
Manufacturer Address : Damastown, Mulhuddart, Dublin 15, Ireland
Registrant Name : Hyundai Pharmaceutical Co., Ltd.
Registration Date : 2015-09-09
Registration Number : 20131029-137-H-241-10(3)
Manufacturer Name : Clarochem Ireland Ltd.
Manufacturer Address : Damastown, Mulhuddart, Dublin 15, Ireland
Registrant Name : Good Pharma Co., Ltd.
Registration Date : 2013-12-30
Registration Number : 20131029-137-H-241-10(1)
Manufacturer Name : Clarochem Ireland Ltd.
Manufacturer Address : Damastown, Mulhuddart, Dublin 15, Ireland
Registrant Name : Hyundai Pharmaceutical Co., Ltd.
Registration Date : 2011-01-31
Registration Number : 20110131-137-H-105-07
Manufacturer Name : AMSA - ANONIMA MATERIE SINTE...
Manufacturer Address : VIA G. DI VITTORIO. 6, 22100 COMO
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
Cosma S.p.A., part of CFM Group with AMSA & Clarochem, provides global pharma & veterinary health with 300+ tons of FDA-approved APIs.
About the Company : Cosma S.p.A., part of the CFM Group along with AMSA and Clarochem Ireland, is the group’s largest manufacturing site, located in Bergamo, Italy. With a 130,000L glass-lined react...
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
About the Company : Cohance Lifesciences is a leading CDMO and API platform, offering products and services across all phases of a molecule’s lifecycle from development to commercialzation. With our...
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...
Lewens Labs transforms healthcare with innovative, sustainable, and affordable pharmaceutical solutions worldwide.
About the Company : Lewens Labs was established with a vision to transform the pharmaceutical industry, inspired by an award-winning engineering project that reduced the cost of Aceclofenac and earned...
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]API Reference Price
API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
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ABOUT THIS PAGE
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PharmaCompass offers a list of Levodropropizine 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 Levodropropizine manufacturer or Levodropropizine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levodropropizine manufacturer or Levodropropizine supplier.
PharmaCompass also assists you with knowing the Levodropropizine API Price utilized in the formulation of products. Levodropropizine API Price is not always fixed or binding as the Levodropropizine Price is obtained through a variety of data sources. The Levodropropizine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Levodropropizine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levodropropizine, including repackagers and relabelers. The FDA regulates Levodropropizine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levodropropizine 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 Levodropropizine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levodropropizine supplier is an individual or a company that provides Levodropropizine active pharmaceutical ingredient (API) or Levodropropizine finished formulations upon request. The Levodropropizine suppliers may include Levodropropizine API manufacturers, exporters, distributors and traders.
click here to find a list of Levodropropizine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Levodropropizine Drug Master File in Korea (Levodropropizine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Levodropropizine. The MFDS reviews the Levodropropizine KDMF as part of the drug registration process and uses the information provided in the Levodropropizine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Levodropropizine 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 Levodropropizine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Levodropropizine suppliers with KDMF on PharmaCompass.
A Levodropropizine CEP of the European Pharmacopoeia monograph is often referred to as a Levodropropizine Certificate of Suitability (COS). The purpose of a Levodropropizine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Levodropropizine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Levodropropizine to their clients by showing that a Levodropropizine CEP has been issued for it. The manufacturer submits a Levodropropizine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Levodropropizine CEP holder for the record. Additionally, the data presented in the Levodropropizine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Levodropropizine DMF.
A Levodropropizine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Levodropropizine 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 Levodropropizine suppliers with CEP (COS) on PharmaCompass.
A Levodropropizine written confirmation (Levodropropizine WC) is an official document issued by a regulatory agency to a Levodropropizine manufacturer, verifying that the manufacturing facility of a Levodropropizine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Levodropropizine APIs or Levodropropizine finished pharmaceutical products to another nation, regulatory agencies frequently require a Levodropropizine WC (written confirmation) as part of the regulatory process.
click here to find a list of Levodropropizine suppliers with Written Confirmation (WC) on PharmaCompass.
Levodropropizine 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 Levodropropizine 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 Levodropropizine GMP manufacturer or Levodropropizine GMP API supplier for your needs.
A Levodropropizine CoA (Certificate of Analysis) is a formal document that attests to Levodropropizine's compliance with Levodropropizine specifications and serves as a tool for batch-level quality control.
Levodropropizine CoA mostly includes findings from lab analyses of a specific batch. For each Levodropropizine 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.
Levodropropizine may be tested according to a variety of international standards, such as European Pharmacopoeia (Levodropropizine EP), Levodropropizine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Levodropropizine USP).
