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API SUPPLIERS
Jai Radhe Sales is your partner for all your sourcing needs.
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USDMF
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Jai Radhe Sales is your partner for all your sourcing needs.
About the Company : Jai Radhe Sales was founded in 1999 as an out-of-the-box distribution firm specializing in the global supply of high-quality pharmaceutical ingredients. The firm provides complete ...
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Regulatory Info :
Registration Country : Switzerland
Brand Name : Kemadrin
Dosage Form : Tabl
Dosage Strength : 5mg
Packaging :
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Regulatory Info :
Registration Country : Switzerland
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Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info :
Registration Country : India
Brand Name : Procyclidine
Dosage Form : Tablet
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
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Regulatory FDF Prices
RX/OTC/DISCN : Class B
Dosage Form : Tabl
Dosage Strength : 5mg
Price Per Pack (Euro) : 8.89
Published in :
Country : Switzerland
RX/OTC/DISCN : Class B
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ABOUT THIS PAGE
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PharmaCompass offers a list of Procyclidine 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 Procyclidine manufacturer or Procyclidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Procyclidine manufacturer or Procyclidine supplier.
PharmaCompass also assists you with knowing the Procyclidine API Price utilized in the formulation of products. Procyclidine API Price is not always fixed or binding as the Procyclidine Price is obtained through a variety of data sources. The Procyclidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Procyclidine HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Procyclidine HCl, including repackagers and relabelers. The FDA regulates Procyclidine HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Procyclidine HCl 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 Procyclidine HCl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Procyclidine HCl supplier is an individual or a company that provides Procyclidine HCl active pharmaceutical ingredient (API) or Procyclidine HCl finished formulations upon request. The Procyclidine HCl suppliers may include Procyclidine HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Procyclidine HCl suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Procyclidine HCl DMF (Drug Master File) is a document detailing the whole manufacturing process of Procyclidine HCl active pharmaceutical ingredient (API) in detail. Different forms of Procyclidine HCl DMFs exist exist since differing nations have different regulations, such as Procyclidine HCl USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Procyclidine HCl DMF submitted to regulatory agencies in the US is known as a USDMF. Procyclidine HCl USDMF includes data on Procyclidine HCl's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Procyclidine HCl USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Procyclidine HCl suppliers with USDMF 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 Procyclidine HCl as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Procyclidine HCl 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 Procyclidine HCl 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 Procyclidine HCl and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Procyclidine HCl NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Procyclidine HCl suppliers with NDC on PharmaCompass.
Procyclidine HCl 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 Procyclidine HCl 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 Procyclidine HCl GMP manufacturer or Procyclidine HCl GMP API supplier for your needs.
A Procyclidine HCl CoA (Certificate of Analysis) is a formal document that attests to Procyclidine HCl's compliance with Procyclidine HCl specifications and serves as a tool for batch-level quality control.
Procyclidine HCl CoA mostly includes findings from lab analyses of a specific batch. For each Procyclidine HCl 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.
Procyclidine HCl may be tested according to a variety of international standards, such as European Pharmacopoeia (Procyclidine HCl EP), Procyclidine HCl JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Procyclidine HCl USP).
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