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USDMF
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
GDUFA
DMF Review : Complete
Rev. Date : 2023-08-22
Pay. Date : 2023-07-17
DMF Number : 37593
Submission : 2022-12-28
Status :
Type : II
With Fermion, start the journey of your innovative API.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4570
Submission : 1982-05-21
Status :
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Complete
Rev. Date : 2012-12-27
Pay. Date : 2012-11-13
DMF Number : 16459
Submission : 2003-03-10
Status :
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7459
Submission : 1988-05-05
Status :
Type : II
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PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
1-(3-chlorophenyl)-4-(3-chloropropyl) piperazine, ...
CAS Number : 52605-52-4
End Use API : Trazodone Hydrochloride
About The Company : PMC Isochem is a CDMO company acquired by PMC International in 2017. It manufactures cGMP intermediates, active pharmaceutical ingredients and functional excipi...
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PharmaCompass offers a list of Trazodone 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 Trazodone Hydrochloride manufacturer or Trazodone Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trazodone Hydrochloride manufacturer or Trazodone Hydrochloride supplier.
PharmaCompass also assists you with knowing the Trazodone Hydrochloride API Price utilized in the formulation of products. Trazodone Hydrochloride API Price is not always fixed or binding as the Trazodone Hydrochloride Price is obtained through a variety of data sources. The Trazodone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trazodone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trazodone Hydrochloride, including repackagers and relabelers. The FDA regulates Trazodone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trazodone 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 Trazodone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trazodone Hydrochloride supplier is an individual or a company that provides Trazodone Hydrochloride active pharmaceutical ingredient (API) or Trazodone Hydrochloride finished formulations upon request. The Trazodone Hydrochloride suppliers may include Trazodone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Trazodone Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Trazodone Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Trazodone Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Trazodone Hydrochloride DMFs exist exist since differing nations have different regulations, such as Trazodone Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Trazodone Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Trazodone Hydrochloride USDMF includes data on Trazodone Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Trazodone Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Trazodone 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 Trazodone Hydrochloride Drug Master File in Japan (Trazodone Hydrochloride JDMF) empowers Trazodone 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 Trazodone Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Trazodone 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 Trazodone Hydrochloride suppliers with JDMF 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 Trazodone Hydrochloride Drug Master File in Korea (Trazodone Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Trazodone Hydrochloride. The MFDS reviews the Trazodone Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Trazodone Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Trazodone Hydrochloride 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 Trazodone Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Trazodone Hydrochloride suppliers with KDMF on PharmaCompass.
A Trazodone Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Trazodone Hydrochloride Certificate of Suitability (COS). The purpose of a Trazodone Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Trazodone Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Trazodone Hydrochloride to their clients by showing that a Trazodone Hydrochloride CEP has been issued for it. The manufacturer submits a Trazodone Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Trazodone Hydrochloride CEP holder for the record. Additionally, the data presented in the Trazodone Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Trazodone Hydrochloride DMF.
A Trazodone Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Trazodone Hydrochloride 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 Trazodone Hydrochloride suppliers with CEP (COS) on PharmaCompass.
A Trazodone Hydrochloride written confirmation (Trazodone Hydrochloride WC) is an official document issued by a regulatory agency to a Trazodone Hydrochloride manufacturer, verifying that the manufacturing facility of a Trazodone Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Trazodone Hydrochloride APIs or Trazodone Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Trazodone Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Trazodone 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 Trazodone Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Trazodone 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 Trazodone 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 Trazodone Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Trazodone Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Trazodone Hydrochloride suppliers with NDC on PharmaCompass.
Trazodone 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 Trazodone 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 Trazodone Hydrochloride GMP manufacturer or Trazodone Hydrochloride GMP API supplier for your needs.
A Trazodone Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Trazodone Hydrochloride's compliance with Trazodone Hydrochloride specifications and serves as a tool for batch-level quality control.
Trazodone Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Trazodone 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.
Trazodone Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Trazodone Hydrochloride EP), Trazodone Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Trazodone Hydrochloride USP).
