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