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