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