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DOSAGE - POWDER;INTRAVENOUS - 175MG/VIAL
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DOSAGE - POWDER;INTRAVENOUS - 300MG/VIAL
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PharmaCompass offers a list of Levoleucovorin 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 Levoleucovorin manufacturer or Levoleucovorin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levoleucovorin manufacturer or Levoleucovorin supplier.
PharmaCompass also assists you with knowing the Levoleucovorin API Price utilized in the formulation of products. Levoleucovorin API Price is not always fixed or binding as the Levoleucovorin Price is obtained through a variety of data sources. The Levoleucovorin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LFP 754 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LFP 754, including repackagers and relabelers. The FDA regulates LFP 754 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LFP 754 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 LFP 754 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LFP 754 supplier is an individual or a company that provides LFP 754 active pharmaceutical ingredient (API) or LFP 754 finished formulations upon request. The LFP 754 suppliers may include LFP 754 API manufacturers, exporters, distributors and traders.
click here to find a list of LFP 754 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A LFP 754 DMF (Drug Master File) is a document detailing the whole manufacturing process of LFP 754 active pharmaceutical ingredient (API) in detail. Different forms of LFP 754 DMFs exist exist since differing nations have different regulations, such as LFP 754 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A LFP 754 DMF submitted to regulatory agencies in the US is known as a USDMF. LFP 754 USDMF includes data on LFP 754's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The LFP 754 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of LFP 754 suppliers with USDMF 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 LFP 754 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for LFP 754 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 LFP 754 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 LFP 754 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a LFP 754 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of LFP 754 suppliers with NDC on PharmaCompass.
LFP 754 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 LFP 754 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 LFP 754 GMP manufacturer or LFP 754 GMP API supplier for your needs.
A LFP 754 CoA (Certificate of Analysis) is a formal document that attests to LFP 754's compliance with LFP 754 specifications and serves as a tool for batch-level quality control.
LFP 754 CoA mostly includes findings from lab analyses of a specific batch. For each LFP 754 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.
LFP 754 may be tested according to a variety of international standards, such as European Pharmacopoeia (LFP 754 EP), LFP 754 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (LFP 754 USP).
