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API SUPPLIERS
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USDMF
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Rochem International Inc
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PharmaCompass offers a list of Sodium Dicloxacillin 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 Sodium Dicloxacillin manufacturer or Sodium Dicloxacillin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Dicloxacillin manufacturer or Sodium Dicloxacillin supplier.
PharmaCompass also assists you with knowing the Sodium Dicloxacillin API Price utilized in the formulation of products. Sodium Dicloxacillin API Price is not always fixed or binding as the Sodium Dicloxacillin Price is obtained through a variety of data sources. The Sodium Dicloxacillin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Diclocil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diclocil, including repackagers and relabelers. The FDA regulates Diclocil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diclocil 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 Diclocil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diclocil supplier is an individual or a company that provides Diclocil active pharmaceutical ingredient (API) or Diclocil finished formulations upon request. The Diclocil suppliers may include Diclocil API manufacturers, exporters, distributors and traders.
click here to find a list of Diclocil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Diclocil DMF (Drug Master File) is a document detailing the whole manufacturing process of Diclocil active pharmaceutical ingredient (API) in detail. Different forms of Diclocil DMFs exist exist since differing nations have different regulations, such as Diclocil USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Diclocil DMF submitted to regulatory agencies in the US is known as a USDMF. Diclocil USDMF includes data on Diclocil's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Diclocil USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Diclocil suppliers with USDMF on PharmaCompass.
A Diclocil CEP of the European Pharmacopoeia monograph is often referred to as a Diclocil Certificate of Suitability (COS). The purpose of a Diclocil CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Diclocil EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Diclocil to their clients by showing that a Diclocil CEP has been issued for it. The manufacturer submits a Diclocil CEP (COS) as part of the market authorization procedure, and it takes on the role of a Diclocil CEP holder for the record. Additionally, the data presented in the Diclocil CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Diclocil DMF.
A Diclocil CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Diclocil CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Diclocil suppliers with CEP (COS) on PharmaCompass.
A Diclocil written confirmation (Diclocil WC) is an official document issued by a regulatory agency to a Diclocil manufacturer, verifying that the manufacturing facility of a Diclocil active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Diclocil APIs or Diclocil finished pharmaceutical products to another nation, regulatory agencies frequently require a Diclocil WC (written confirmation) as part of the regulatory process.
click here to find a list of Diclocil suppliers with Written Confirmation (WC) 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 Diclocil as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Diclocil 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 Diclocil 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 Diclocil and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Diclocil NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Diclocil suppliers with NDC on PharmaCompass.
Diclocil 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 Diclocil 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 Diclocil GMP manufacturer or Diclocil GMP API supplier for your needs.
A Diclocil CoA (Certificate of Analysis) is a formal document that attests to Diclocil's compliance with Diclocil specifications and serves as a tool for batch-level quality control.
Diclocil CoA mostly includes findings from lab analyses of a specific batch. For each Diclocil 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.
Diclocil may be tested according to a variety of international standards, such as European Pharmacopoeia (Diclocil EP), Diclocil JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Diclocil USP).
