Synopsis
0
CEP/COS
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Europe
0
Canada
0
Australia
0
South Africa
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]API Reference Price
API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
38
PharmaCompass offers a list of Ritodrine 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 Ritodrine Hydrochloride manufacturer or Ritodrine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ritodrine Hydrochloride manufacturer or Ritodrine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Ritodrine Hydrochloride API Price utilized in the formulation of products. Ritodrine Hydrochloride API Price is not always fixed or binding as the Ritodrine Hydrochloride Price is obtained through a variety of data sources. The Ritodrine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Utopar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Utopar, including repackagers and relabelers. The FDA regulates Utopar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Utopar 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 Utopar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Utopar supplier is an individual or a company that provides Utopar active pharmaceutical ingredient (API) or Utopar finished formulations upon request. The Utopar suppliers may include Utopar API manufacturers, exporters, distributors and traders.
click here to find a list of Utopar suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Utopar DMF (Drug Master File) is a document detailing the whole manufacturing process of Utopar active pharmaceutical ingredient (API) in detail. Different forms of Utopar DMFs exist exist since differing nations have different regulations, such as Utopar USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Utopar DMF submitted to regulatory agencies in the US is known as a USDMF. Utopar USDMF includes data on Utopar's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Utopar USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Utopar 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 Utopar Drug Master File in Japan (Utopar JDMF) empowers Utopar 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 Utopar JDMF during the approval evaluation for pharmaceutical products. At the time of Utopar 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 Utopar suppliers with JDMF on PharmaCompass.
Utopar 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 Utopar 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 Utopar GMP manufacturer or Utopar GMP API supplier for your needs.
A Utopar CoA (Certificate of Analysis) is a formal document that attests to Utopar's compliance with Utopar specifications and serves as a tool for batch-level quality control.
Utopar CoA mostly includes findings from lab analyses of a specific batch. For each Utopar 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.
Utopar may be tested according to a variety of international standards, such as European Pharmacopoeia (Utopar EP), Utopar JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Utopar USP).
