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API SUPPLIERS
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Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
About the Company : Rochem, established in 1994, is a global distributor of pharmaceutical, food, nutritional, and animal health ingredients, sourcing high-quality products from China. Headquartered i...
Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
About the Company : Established in 1991, Pharm-Rx is an importer and distributor of active ingredients serving the pharmaceutical, nutritional supplement, and food industries. The company follows a hi...
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
About the Company : Octavius Pharma is a global leader in Directly Compressible Granules with over 45 years of experience in formulation development, manufacturing, and commercialization. Its portfoli...
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
About the Company : Tenatra International was established as a proprietorship firm in 1999. It got off to a very good start, supporting clients in the United States, Mexico and Europe. As business opp...
Willow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.
About the Company : Willow Birch Pharma, Inc. is a premier supplier of bulk APIs to North American Compounding Pharmacies, sourcing from FDA registered and GMP manufacturers. With licenses in all 50 s...
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PharmaCompass offers a list of Aluminium Hydroxide 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 Aluminium Hydroxide manufacturer or Aluminium Hydroxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aluminium Hydroxide manufacturer or Aluminium Hydroxide supplier.
PharmaCompass also assists you with knowing the Aluminium Hydroxide API Price utilized in the formulation of products. Aluminium Hydroxide API Price is not always fixed or binding as the Aluminium Hydroxide Price is obtained through a variety of data sources. The Aluminium Hydroxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Algeldratum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Algeldratum, including repackagers and relabelers. The FDA regulates Algeldratum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Algeldratum 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 Algeldratum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Algeldratum supplier is an individual or a company that provides Algeldratum active pharmaceutical ingredient (API) or Algeldratum finished formulations upon request. The Algeldratum suppliers may include Algeldratum API manufacturers, exporters, distributors and traders.
click here to find a list of Algeldratum suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Algeldratum DMF (Drug Master File) is a document detailing the whole manufacturing process of Algeldratum active pharmaceutical ingredient (API) in detail. Different forms of Algeldratum DMFs exist exist since differing nations have different regulations, such as Algeldratum USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Algeldratum DMF submitted to regulatory agencies in the US is known as a USDMF. Algeldratum USDMF includes data on Algeldratum's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Algeldratum USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Algeldratum suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Algeldratum Drug Master File in Japan (Algeldratum JDMF) empowers Algeldratum API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Algeldratum JDMF during the approval evaluation for pharmaceutical products. At the time of Algeldratum JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Algeldratum suppliers with JDMF on PharmaCompass.
A Algeldratum written confirmation (Algeldratum WC) is an official document issued by a regulatory agency to a Algeldratum manufacturer, verifying that the manufacturing facility of a Algeldratum active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Algeldratum APIs or Algeldratum finished pharmaceutical products to another nation, regulatory agencies frequently require a Algeldratum WC (written confirmation) as part of the regulatory process.
click here to find a list of Algeldratum 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 Algeldratum as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Algeldratum 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 Algeldratum 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 Algeldratum and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Algeldratum NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Algeldratum suppliers with NDC on PharmaCompass.
Algeldratum 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 Algeldratum 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 Algeldratum GMP manufacturer or Algeldratum GMP API supplier for your needs.
A Algeldratum CoA (Certificate of Analysis) is a formal document that attests to Algeldratum's compliance with Algeldratum specifications and serves as a tool for batch-level quality control.
Algeldratum CoA mostly includes findings from lab analyses of a specific batch. For each Algeldratum 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.
Algeldratum may be tested according to a variety of international standards, such as European Pharmacopoeia (Algeldratum EP), Algeldratum JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Algeldratum USP).
