X
API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
Other Suppliers
0
USA (Orange Book)
Europe
Canada
0
Australia
South Africa
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
55
PharmaCompass offers a list of Ranitidine 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 Ranitidine manufacturer or Ranitidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ranitidine manufacturer or Ranitidine supplier.
PharmaCompass also assists you with knowing the Ranitidine API Price utilized in the formulation of products. Ranitidine API Price is not always fixed or binding as the Ranitidine Price is obtained through a variety of data sources. The Ranitidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ranitidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ranitidine, including repackagers and relabelers. The FDA regulates Ranitidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ranitidine 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 Ranitidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ranitidine supplier is an individual or a company that provides Ranitidine active pharmaceutical ingredient (API) or Ranitidine finished formulations upon request. The Ranitidine suppliers may include Ranitidine API manufacturers, exporters, distributors and traders.
click here to find a list of Ranitidine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ranitidine DMF (Drug Master File) is a document detailing the whole manufacturing process of Ranitidine active pharmaceutical ingredient (API) in detail. Different forms of Ranitidine DMFs exist exist since differing nations have different regulations, such as Ranitidine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ranitidine DMF submitted to regulatory agencies in the US is known as a USDMF. Ranitidine USDMF includes data on Ranitidine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ranitidine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ranitidine suppliers with USDMF on PharmaCompass.
A Ranitidine written confirmation (Ranitidine WC) is an official document issued by a regulatory agency to a Ranitidine manufacturer, verifying that the manufacturing facility of a Ranitidine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ranitidine APIs or Ranitidine finished pharmaceutical products to another nation, regulatory agencies frequently require a Ranitidine WC (written confirmation) as part of the regulatory process.
click here to find a list of Ranitidine suppliers with Written Confirmation (WC) on PharmaCompass.
Ranitidine 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 Ranitidine 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 Ranitidine GMP manufacturer or Ranitidine GMP API supplier for your needs.
A Ranitidine CoA (Certificate of Analysis) is a formal document that attests to Ranitidine's compliance with Ranitidine specifications and serves as a tool for batch-level quality control.
Ranitidine CoA mostly includes findings from lab analyses of a specific batch. For each Ranitidine 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.
Ranitidine may be tested according to a variety of international standards, such as European Pharmacopoeia (Ranitidine EP), Ranitidine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ranitidine USP).
Market Place
