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