Synopsis
DRUG PRODUCT COMPOSITIONS
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
API SUPPLIERS
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USDMF
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EUROAPI
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Evonik
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]SPI Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Seqens
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Dosage Form : Injectable / Parenteral
Grade : Parenteral
Brand Name : Expansorb® PCL Polymers
Application : Parenteral
Excipient Details : Poly (caprolactone) polymers are used as functional excipients for controlled and slow drug release (weeks to months) with a single injection.
Pharmacopoeia Ref : N/A
Technical Specs : Classic and ultrapure LMP
Ingredient(s) : Caprolactone Excipient
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Boai NKY Pharmaceuticals Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Healthcare
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nanjing Well Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shanghai Minbiotech
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Kirsch Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Dr. Paul Lohmann GmbH & Co. KGaA
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Actylis
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Aeon Procare
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Anhui Sunhere Pharmaceutical Excipients Co.,Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Ashland
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]BioSpectra
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]CD Formulation
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Clariant
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Corel Pharma Chem
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DFE Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Esteem Industries
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Finar
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Chemicals
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gloria Interchem
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Ideal Cures
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Ingredion Pharma Solutions
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Kerry
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Keval Exports
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Lubrizol Life Science Health
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Microlex e.U
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nanjing Bold Chemical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Neelkanth MineChem
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nippon Fine Chemical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nitika Pharmaceutical Specialities
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Novo Excipients
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pharmatrans-Sanaq
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pluviaendo
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Prachin Chemical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Roquette
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Seppic
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shanghai Shenmei Pharmaceutical Technology Co., Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Sigachi Industries
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Silverline Chemicals
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Symrise
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Topical
Solubilizers
Fillers, Diluents & Binders
Parenteral
Thickeners and Stabilizers
Emulsifying Agents
Lubricants & Glidants
Granulation
Direct Compression
Surfactant & Foaming Agents
Coating Systems & Additives
Disintegrants & Superdisintegrants
Film Formers & Plasticizers
Co-Processed Excipients
API Stability Enhancers
Controlled & Modified Release
Taste Masking
Rheology Modifiers
Chewable & Orodispersible Aids
Digital Content
DATA COMPILATION #PharmaFlow
NEWS #PharmaBuzz
Global Sales Information
US Medicaid Prescriptions
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US Patents
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ABOUT THIS PAGE
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PharmaCompass offers a list of Clotrimazole 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 Clotrimazole manufacturer or Clotrimazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clotrimazole manufacturer or Clotrimazole supplier.
PharmaCompass also assists you with knowing the Clotrimazole API Price utilized in the formulation of products. Clotrimazole API Price is not always fixed or binding as the Clotrimazole Price is obtained through a variety of data sources. The Clotrimazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gyne lotrimin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gyne lotrimin, including repackagers and relabelers. The FDA regulates Gyne lotrimin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gyne lotrimin 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 Gyne lotrimin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gyne lotrimin supplier is an individual or a company that provides Gyne lotrimin active pharmaceutical ingredient (API) or Gyne lotrimin finished formulations upon request. The Gyne lotrimin suppliers may include Gyne lotrimin API manufacturers, exporters, distributors and traders.
click here to find a list of Gyne lotrimin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gyne lotrimin DMF (Drug Master File) is a document detailing the whole manufacturing process of Gyne lotrimin active pharmaceutical ingredient (API) in detail. Different forms of Gyne lotrimin DMFs exist exist since differing nations have different regulations, such as Gyne lotrimin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Gyne lotrimin DMF submitted to regulatory agencies in the US is known as a USDMF. Gyne lotrimin USDMF includes data on Gyne lotrimin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Gyne lotrimin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Gyne lotrimin 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 Gyne lotrimin Drug Master File in Japan (Gyne lotrimin JDMF) empowers Gyne lotrimin 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 Gyne lotrimin JDMF during the approval evaluation for pharmaceutical products. At the time of Gyne lotrimin 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 Gyne lotrimin 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 Gyne lotrimin Drug Master File in Korea (Gyne lotrimin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Gyne lotrimin. The MFDS reviews the Gyne lotrimin KDMF as part of the drug registration process and uses the information provided in the Gyne lotrimin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Gyne lotrimin 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 Gyne lotrimin API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Gyne lotrimin suppliers with KDMF on PharmaCompass.
A Gyne lotrimin CEP of the European Pharmacopoeia monograph is often referred to as a Gyne lotrimin Certificate of Suitability (COS). The purpose of a Gyne lotrimin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Gyne lotrimin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Gyne lotrimin to their clients by showing that a Gyne lotrimin CEP has been issued for it. The manufacturer submits a Gyne lotrimin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Gyne lotrimin CEP holder for the record. Additionally, the data presented in the Gyne lotrimin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Gyne lotrimin DMF.
A Gyne lotrimin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Gyne lotrimin 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 Gyne lotrimin suppliers with CEP (COS) on PharmaCompass.
A Gyne lotrimin written confirmation (Gyne lotrimin WC) is an official document issued by a regulatory agency to a Gyne lotrimin manufacturer, verifying that the manufacturing facility of a Gyne lotrimin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Gyne lotrimin APIs or Gyne lotrimin finished pharmaceutical products to another nation, regulatory agencies frequently require a Gyne lotrimin WC (written confirmation) as part of the regulatory process.
click here to find a list of Gyne lotrimin 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 Gyne lotrimin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Gyne lotrimin 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 Gyne lotrimin 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 Gyne lotrimin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Gyne lotrimin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Gyne lotrimin suppliers with NDC on PharmaCompass.
Gyne lotrimin 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 Gyne lotrimin 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 Gyne lotrimin GMP manufacturer or Gyne lotrimin GMP API supplier for your needs.
A Gyne lotrimin CoA (Certificate of Analysis) is a formal document that attests to Gyne lotrimin's compliance with Gyne lotrimin specifications and serves as a tool for batch-level quality control.
Gyne lotrimin CoA mostly includes findings from lab analyses of a specific batch. For each Gyne lotrimin 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.
Gyne lotrimin may be tested according to a variety of international standards, such as European Pharmacopoeia (Gyne lotrimin EP), Gyne lotrimin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Gyne lotrimin USP).
