Synopsis
0
JDMF
0
KDMF
0
VMF
0
EDQM
0
USP
0
JP
0
Others
0
Australia
0
South Africa
DRUG PRODUCT COMPOSITIONS0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]CEP/COS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results] EU WC
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Drugs in Development
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDA Orange Book
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Europe
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DRUG PRODUCT COMPOSITIONS
DOSAGE - INJECTABLE;INJECTION - 20MG/ML **Fed...DOSAGE - INJECTABLE;INJECTION - 20MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 16466
DOSAGE - INJECTABLE;INJECTION - 5MG/ML **Fede...DOSAGE - INJECTABLE;INJECTION - 5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 16466
Related Excipient Companies
Rochem International Inc
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]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]Actylis
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]Nanjing Bold 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]Shijiazhuang Huaxu Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Zhejiang Huakang Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Solubilizers
Film Formers & Plasticizers
Parenteral
Topical
Fillers, Diluents & Binders
Taste Masking
Coating Systems & Additives
Emulsifying Agents
Direct Compression
Co-Processed Excipients
Surfactant & Foaming Agents
Chewable & Orodispersible Aids
Thickeners and Stabilizers
Soft Gelatin
Rheology Modifiers
API Stability Enhancers
Market Place
ABOUT THIS PAGE
89
PharmaCompass offers a list of Triamcinolone Hexacetonide 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 Triamcinolone Hexacetonide manufacturer or Triamcinolone Hexacetonide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Triamcinolone Hexacetonide manufacturer or Triamcinolone Hexacetonide supplier.
PharmaCompass also assists you with knowing the Triamcinolone Hexacetonide API Price utilized in the formulation of products. Triamcinolone Hexacetonide API Price is not always fixed or binding as the Triamcinolone Hexacetonide Price is obtained through a variety of data sources. The Triamcinolone Hexacetonide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aristospan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aristospan, including repackagers and relabelers. The FDA regulates Aristospan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aristospan 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 Aristospan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aristospan supplier is an individual or a company that provides Aristospan active pharmaceutical ingredient (API) or Aristospan finished formulations upon request. The Aristospan suppliers may include Aristospan API manufacturers, exporters, distributors and traders.
click here to find a list of Aristospan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aristospan DMF (Drug Master File) is a document detailing the whole manufacturing process of Aristospan active pharmaceutical ingredient (API) in detail. Different forms of Aristospan DMFs exist exist since differing nations have different regulations, such as Aristospan USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Aristospan DMF submitted to regulatory agencies in the US is known as a USDMF. Aristospan USDMF includes data on Aristospan's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Aristospan USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Aristospan suppliers with USDMF on PharmaCompass.
A Aristospan CEP of the European Pharmacopoeia monograph is often referred to as a Aristospan Certificate of Suitability (COS). The purpose of a Aristospan CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aristospan EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aristospan to their clients by showing that a Aristospan CEP has been issued for it. The manufacturer submits a Aristospan CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aristospan CEP holder for the record. Additionally, the data presented in the Aristospan CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aristospan DMF.
A Aristospan CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aristospan 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 Aristospan suppliers with CEP (COS) on PharmaCompass.
A Aristospan written confirmation (Aristospan WC) is an official document issued by a regulatory agency to a Aristospan manufacturer, verifying that the manufacturing facility of a Aristospan active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Aristospan APIs or Aristospan finished pharmaceutical products to another nation, regulatory agencies frequently require a Aristospan WC (written confirmation) as part of the regulatory process.
click here to find a list of Aristospan 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 Aristospan as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Aristospan 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 Aristospan 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 Aristospan and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Aristospan NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Aristospan suppliers with NDC on PharmaCompass.
Aristospan 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 Aristospan 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 Aristospan GMP manufacturer or Aristospan GMP API supplier for your needs.
A Aristospan CoA (Certificate of Analysis) is a formal document that attests to Aristospan's compliance with Aristospan specifications and serves as a tool for batch-level quality control.
Aristospan CoA mostly includes findings from lab analyses of a specific batch. For each Aristospan 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.
Aristospan may be tested according to a variety of international standards, such as European Pharmacopoeia (Aristospan EP), Aristospan JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Aristospan USP).
