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ABOUT THIS PAGE
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PharmaCompass offers a list of Tobramycin Sulfate 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 Tobramycin Sulfate manufacturer or Tobramycin Sulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tobramycin Sulfate manufacturer or Tobramycin Sulfate supplier.
PharmaCompass also assists you with knowing the Tobramycin Sulfate API Price utilized in the formulation of products. Tobramycin Sulfate API Price is not always fixed or binding as the Tobramycin Sulfate Price is obtained through a variety of data sources. The Tobramycin Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dicon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dicon, including repackagers and relabelers. The FDA regulates Dicon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dicon 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 Dicon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dicon supplier is an individual or a company that provides Dicon active pharmaceutical ingredient (API) or Dicon finished formulations upon request. The Dicon suppliers may include Dicon API manufacturers, exporters, distributors and traders.
click here to find a list of Dicon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dicon DMF (Drug Master File) is a document detailing the whole manufacturing process of Dicon active pharmaceutical ingredient (API) in detail. Different forms of Dicon DMFs exist exist since differing nations have different regulations, such as Dicon USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dicon DMF submitted to regulatory agencies in the US is known as a USDMF. Dicon USDMF includes data on Dicon's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dicon USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dicon 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 Dicon Drug Master File in Japan (Dicon JDMF) empowers Dicon 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 Dicon JDMF during the approval evaluation for pharmaceutical products. At the time of Dicon 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 Dicon suppliers with JDMF 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 Dicon Drug Master File in Korea (Dicon KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Dicon. The MFDS reviews the Dicon KDMF as part of the drug registration process and uses the information provided in the Dicon KDMF to evaluate the safety and efficacy of the drug.
After submitting a Dicon 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 Dicon API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Dicon suppliers with KDMF 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 Dicon as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Dicon 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 Dicon 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 Dicon and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Dicon NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Dicon suppliers with NDC on PharmaCompass.
Dicon 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 Dicon 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 Dicon GMP manufacturer or Dicon GMP API supplier for your needs.
A Dicon CoA (Certificate of Analysis) is a formal document that attests to Dicon's compliance with Dicon specifications and serves as a tool for batch-level quality control.
Dicon CoA mostly includes findings from lab analyses of a specific batch. For each Dicon 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.
Dicon may be tested according to a variety of international standards, such as European Pharmacopoeia (Dicon EP), Dicon JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dicon USP).
