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API SUPPLIERS
Century has been an API manufacturer for over 40 years & is the partner of choice for multipurpose custom manufacturing projects.
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
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USDMF
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API Imports and Exports
INTERMEDIATE SUPPLIERS
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
CAS Number : 8011-61-8
End Use API : Gramicidin
About The Company : Headquartered in Fengxian District, Shanghai Minbiotech Co., Ltd. is a company specializing in the R&D and production of advanced pharmaceutical intermediate...
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Nanjing Well Pharmaceutical
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Solubilizers
Thickeners and Stabilizers
Parenteral
Controlled & Modified Release
Film Formers & Plasticizers
Granulation
Emulsifying Agents
Direct Compression
Coating Systems & Additives
Global Sales Information
US Medicaid Prescriptions
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REF. STANDARDS & IMPURITIES
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PharmaCompass offers a list of Gramicidin 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 Gramicidin manufacturer or Gramicidin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gramicidin manufacturer or Gramicidin supplier.
PharmaCompass also assists you with knowing the Gramicidin API Price utilized in the formulation of products. Gramicidin API Price is not always fixed or binding as the Gramicidin Price is obtained through a variety of data sources. The Gramicidin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NEOSPORIN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NEOSPORIN, including repackagers and relabelers. The FDA regulates NEOSPORIN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NEOSPORIN 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 NEOSPORIN manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A NEOSPORIN supplier is an individual or a company that provides NEOSPORIN active pharmaceutical ingredient (API) or NEOSPORIN finished formulations upon request. The NEOSPORIN suppliers may include NEOSPORIN API manufacturers, exporters, distributors and traders.
click here to find a list of NEOSPORIN suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A NEOSPORIN DMF (Drug Master File) is a document detailing the whole manufacturing process of NEOSPORIN active pharmaceutical ingredient (API) in detail. Different forms of NEOSPORIN DMFs exist exist since differing nations have different regulations, such as NEOSPORIN USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A NEOSPORIN DMF submitted to regulatory agencies in the US is known as a USDMF. NEOSPORIN USDMF includes data on NEOSPORIN's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The NEOSPORIN USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of NEOSPORIN 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 NEOSPORIN Drug Master File in Japan (NEOSPORIN JDMF) empowers NEOSPORIN 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 NEOSPORIN JDMF during the approval evaluation for pharmaceutical products. At the time of NEOSPORIN 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 NEOSPORIN suppliers with JDMF on PharmaCompass.
A NEOSPORIN CEP of the European Pharmacopoeia monograph is often referred to as a NEOSPORIN Certificate of Suitability (COS). The purpose of a NEOSPORIN CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of NEOSPORIN EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of NEOSPORIN to their clients by showing that a NEOSPORIN CEP has been issued for it. The manufacturer submits a NEOSPORIN CEP (COS) as part of the market authorization procedure, and it takes on the role of a NEOSPORIN CEP holder for the record. Additionally, the data presented in the NEOSPORIN CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the NEOSPORIN DMF.
A NEOSPORIN CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. NEOSPORIN 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 NEOSPORIN 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 NEOSPORIN as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for NEOSPORIN 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 NEOSPORIN 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 NEOSPORIN and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a NEOSPORIN NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of NEOSPORIN suppliers with NDC on PharmaCompass.
NEOSPORIN 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 NEOSPORIN 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 NEOSPORIN GMP manufacturer or NEOSPORIN GMP API supplier for your needs.
A NEOSPORIN CoA (Certificate of Analysis) is a formal document that attests to NEOSPORIN's compliance with NEOSPORIN specifications and serves as a tool for batch-level quality control.
NEOSPORIN CoA mostly includes findings from lab analyses of a specific batch. For each NEOSPORIN 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.
NEOSPORIN may be tested according to a variety of international standards, such as European Pharmacopoeia (NEOSPORIN EP), NEOSPORIN JP (Japanese Pharmacopeia) and the US Pharmacopoeia (NEOSPORIN USP).
