X
API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
Other Certificates
0
Other Suppliers
0
USA (Orange Book)
0
Europe
0
Canada
0
Australia
0
South Africa
0
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
0
USFDA Orange Book Patents
0
USFDA Exclusivities
0
Blog #PharmaFlow
0
News
0
EDQM
0
USP
0
JP
0
Other Listed Suppliers
0
0
11
PharmaCompass offers a list of L-Carnitine HCl 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 L-Carnitine HCl manufacturer or L-Carnitine HCl supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred L-Carnitine HCl manufacturer or L-Carnitine HCl supplier.
PharmaCompass also assists you with knowing the L-Carnitine HCl API Price utilized in the formulation of products. L-Carnitine HCl API Price is not always fixed or binding as the L-Carnitine HCl Price is obtained through a variety of data sources. The L-Carnitine HCl Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide, including repackagers and relabelers. The FDA regulates 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide 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 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide supplier is an individual or a company that provides 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide active pharmaceutical ingredient (API) or 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide finished formulations upon request. The 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide suppliers may include 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide API manufacturers, exporters, distributors and traders.
click here to find a list of 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide DMF (Drug Master File) is a document detailing the whole manufacturing process of 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide active pharmaceutical ingredient (API) in detail. Different forms of 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide DMFs exist exist since differing nations have different regulations, such as 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide DMF submitted to regulatory agencies in the US is known as a USDMF. 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide USDMF includes data on 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide 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 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide Drug Master File in Japan (1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide JDMF) empowers 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide 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 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide JDMF during the approval evaluation for pharmaceutical products. At the time of 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide 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 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide suppliers with JDMF on PharmaCompass.
1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide 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 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide 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 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide GMP manufacturer or 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide GMP API supplier for your needs.
A 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide CoA (Certificate of Analysis) is a formal document that attests to 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide's compliance with 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide specifications and serves as a tool for batch-level quality control.
1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide CoA mostly includes findings from lab analyses of a specific batch. For each 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide 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.
1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide may be tested according to a variety of international standards, such as European Pharmacopoeia (1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide EP), 1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1-propanaminium-3-carboxy-2-hydroxy-N,N,N-trimethyl hydroxide USP).
Market Place
