API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
0
0
USA (Orange Book)
0
Europe
0
Canada
0
Australia
0
South Africa
0
Uploaded Dossiers
0
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
40
PharmaCompass offers a list of Cascara 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 Cascara manufacturer or Cascara supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cascara manufacturer or Cascara supplier.
PharmaCompass also assists you with knowing the Cascara API Price utilized in the formulation of products. Cascara API Price is not always fixed or binding as the Cascara Price is obtained through a variety of data sources. The Cascara Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cascara manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cascara, including repackagers and relabelers. The FDA regulates Cascara manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cascara 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 Cascara manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cascara supplier is an individual or a company that provides Cascara active pharmaceutical ingredient (API) or Cascara finished formulations upon request. The Cascara suppliers may include Cascara API manufacturers, exporters, distributors and traders.
click here to find a list of Cascara suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cascara DMF (Drug Master File) is a document detailing the whole manufacturing process of Cascara active pharmaceutical ingredient (API) in detail. Different forms of Cascara DMFs exist exist since differing nations have different regulations, such as Cascara USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cascara DMF submitted to regulatory agencies in the US is known as a USDMF. Cascara USDMF includes data on Cascara's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cascara USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cascara suppliers with USDMF on PharmaCompass.
Cascara 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 Cascara 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 Cascara GMP manufacturer or Cascara GMP API supplier for your needs.
A Cascara CoA (Certificate of Analysis) is a formal document that attests to Cascara's compliance with Cascara specifications and serves as a tool for batch-level quality control.
Cascara CoA mostly includes findings from lab analyses of a specific batch. For each Cascara 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.
Cascara may be tested according to a variety of international standards, such as European Pharmacopoeia (Cascara EP), Cascara JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cascara USP).