Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
VMF
0
EDQM
0
USP
0
JP
0
Others
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Canada
0
Australia
0
South Africa
DRUG PRODUCT COMPOSITIONS
0
Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
API SUPPLIERS
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
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USDMF
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API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
Drugs in Development
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Athena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.
Regulatory Info :
Registration Country : France
Brand Name :
Dosage Form : Taste Masked Pellets S...
Dosage Strength : 2G
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
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Evonik
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Dosage Form : Tablet
Grade : Oral
Brand Name : EUDRAGIT® FL 30 D-55
Application : Coating Systems & Additives
Excipient Details : EUDRAGIT® FL 30 D-55 (aqueous dispersion of a combination polymers) is used OSDs coating without addition of plasticizer, utilizing AEMP technology.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Dosage Form : Tablet
Grade : Oral
Brand Name : EUDRAGIT® NE 30 D
Application : Coating Systems & Additives
Excipient Details : Eudragit NE 30 D (aqueous dispersion) is a highly flexible sustained release polymer used for coating (without plasticizer) in OSDs.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Dosage Form : Tablet
Grade : Oral
Brand Name : EUDRAGIT® NE 40 D
Application : Coating Systems & Additives
Excipient Details : EUDRAGIT® NE 40 D (aqueous dispersion) is a sustained release polymer used for coating tablets, granules and pellets.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Dosage Form : Tablet
Grade : Oral
Brand Name : EUDRAGIT® RL 30 D
Application : Controlled & Modified Release
Excipient Details : Eudragit RL 30 D(aqueous dispersion) is a sustained release polymer for customized release profiles, used in combination with EUDRAGIT® RS.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Dosage Form : Tablet
Grade : Oral
Brand Name : EUDRAGIT® RS 12,5
Application : Controlled & Modified Release
Excipient Details : EUDRAGIT® RS 12,5 (Organic solution) is a sustained release polymer for customized release profiles used in combination with EUDRAGIT® RL.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Dosage Form : Tablet
Grade : Oral
Brand Name : EUDRAGIT® RS 30 D
Application : Controlled & Modified Release
Excipient Details : EUDRAGIT® RS 30 D(aqueous dispersion) is a sustained release polymer for customized release profiles used in combination with EUDRAGIT® RL.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Faran Shimi Pharmaceutical
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Solubilizers
Nanjing Well is focused on R&D, production & sales of Pharmaceutical Excipients & Synthetic Lubricating base oils.
Dosage Form : Capsule, Cream / Lotion / Ointment, Gel, Injectable / Parenteral, Solution, Tablet
Grade : Parenteral, Topical, Oral
Brand Name : Polyethylene Glycol 4000
Application : Fillers, Diluents & Binders, Film Formers & Plasticizers, Lubricants & Glidants, Parenteral, Solubilizers, Surfactant & Foaming Agents, Thickeners and Stabilizers, Topical
Excipient Details : PEG 4000 is used as a thickener & suspending agent in suspension injections. It is also used as plasticizer, binder, lubricant & solubilizer.
Fillers, Diluents & Binders
Coating Systems & Additives
Granulation
Parenteral
Thickeners and Stabilizers
Film Formers & Plasticizers
Lubricants & Glidants
Direct Compression
Topical
Taste Masking
Surfactant & Foaming Agents
Emulsifying Agents
Disintegrants & Superdisintegrants
Digital Content
NEWS #PharmaBuzz
Global Sales Information
US Medicaid Prescriptions
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APIs
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FDF DOSSIERS
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21 May 2018
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ABOUT THIS PAGE
53
PharmaCompass offers a list of Secnidazole 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 Secnidazole manufacturer or Secnidazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Secnidazole manufacturer or Secnidazole supplier.
PharmaCompass also assists you with knowing the Secnidazole API Price utilized in the formulation of products. Secnidazole API Price is not always fixed or binding as the Secnidazole Price is obtained through a variety of data sources. The Secnidazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Secnidazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Secnidazole, including repackagers and relabelers. The FDA regulates Secnidazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Secnidazole 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 Secnidazole manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Secnidazole supplier is an individual or a company that provides Secnidazole active pharmaceutical ingredient (API) or Secnidazole finished formulations upon request. The Secnidazole suppliers may include Secnidazole API manufacturers, exporters, distributors and traders.
click here to find a list of Secnidazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Secnidazole DMF (Drug Master File) is a document detailing the whole manufacturing process of Secnidazole active pharmaceutical ingredient (API) in detail. Different forms of Secnidazole DMFs exist exist since differing nations have different regulations, such as Secnidazole USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Secnidazole DMF submitted to regulatory agencies in the US is known as a USDMF. Secnidazole USDMF includes data on Secnidazole's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Secnidazole USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Secnidazole suppliers with USDMF 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 Secnidazole as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Secnidazole 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 Secnidazole 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 Secnidazole and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Secnidazole NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Secnidazole suppliers with NDC on PharmaCompass.
Secnidazole 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 Secnidazole 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 Secnidazole GMP manufacturer or Secnidazole GMP API supplier for your needs.
A Secnidazole CoA (Certificate of Analysis) is a formal document that attests to Secnidazole's compliance with Secnidazole specifications and serves as a tool for batch-level quality control.
Secnidazole CoA mostly includes findings from lab analyses of a specific batch. For each Secnidazole 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.
Secnidazole may be tested according to a variety of international standards, such as European Pharmacopoeia (Secnidazole EP), Secnidazole JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Secnidazole USP).
Comment (3)
