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PharmaCompass offers a list of Doxycycline 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 Doxycycline manufacturer or Doxycycline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Doxycycline manufacturer or Doxycycline supplier.
PharmaCompass also assists you with knowing the Doxycycline API Price utilized in the formulation of products. Doxycycline API Price is not always fixed or binding as the Doxycycline Price is obtained through a variety of data sources. The Doxycycline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Doxycycline Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Doxycycline Monohydrate, including repackagers and relabelers. The FDA regulates Doxycycline Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Doxycycline Monohydrate 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 Doxycycline Monohydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Doxycycline Monohydrate supplier is an individual or a company that provides Doxycycline Monohydrate active pharmaceutical ingredient (API) or Doxycycline Monohydrate finished formulations upon request. The Doxycycline Monohydrate suppliers may include Doxycycline Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Doxycycline Monohydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Doxycycline Monohydrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Doxycycline Monohydrate active pharmaceutical ingredient (API) in detail. Different forms of Doxycycline Monohydrate DMFs exist exist since differing nations have different regulations, such as Doxycycline Monohydrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Doxycycline Monohydrate DMF submitted to regulatory agencies in the US is known as a USDMF. Doxycycline Monohydrate USDMF includes data on Doxycycline Monohydrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Doxycycline Monohydrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Doxycycline Monohydrate suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Doxycycline Monohydrate Drug Master File in Korea (Doxycycline Monohydrate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Doxycycline Monohydrate. The MFDS reviews the Doxycycline Monohydrate KDMF as part of the drug registration process and uses the information provided in the Doxycycline Monohydrate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Doxycycline Monohydrate KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Doxycycline Monohydrate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Doxycycline Monohydrate suppliers with KDMF on PharmaCompass.
A Doxycycline Monohydrate CEP of the European Pharmacopoeia monograph is often referred to as a Doxycycline Monohydrate Certificate of Suitability (COS). The purpose of a Doxycycline Monohydrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Doxycycline Monohydrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Doxycycline Monohydrate to their clients by showing that a Doxycycline Monohydrate CEP has been issued for it. The manufacturer submits a Doxycycline Monohydrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Doxycycline Monohydrate CEP holder for the record. Additionally, the data presented in the Doxycycline Monohydrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Doxycycline Monohydrate DMF.
A Doxycycline Monohydrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Doxycycline Monohydrate 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 Doxycycline Monohydrate 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 Doxycycline Monohydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Doxycycline Monohydrate 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 Doxycycline Monohydrate 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 Doxycycline Monohydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Doxycycline Monohydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Doxycycline Monohydrate suppliers with NDC on PharmaCompass.
Doxycycline Monohydrate 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 Doxycycline Monohydrate 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 Doxycycline Monohydrate GMP manufacturer or Doxycycline Monohydrate GMP API supplier for your needs.
A Doxycycline Monohydrate CoA (Certificate of Analysis) is a formal document that attests to Doxycycline Monohydrate's compliance with Doxycycline Monohydrate specifications and serves as a tool for batch-level quality control.
Doxycycline Monohydrate CoA mostly includes findings from lab analyses of a specific batch. For each Doxycycline Monohydrate 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.
Doxycycline Monohydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Doxycycline Monohydrate EP), Doxycycline Monohydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Doxycycline Monohydrate USP).