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