Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
VMF
0
Listed Suppliers
0
FDF
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
Related Excipient Companies
Rochem International Inc
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pharm-RX Chemical
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]Actylis
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]Gangwal Chemicals
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Ideal Cures Pvt Ltd
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]Pluviaendo
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shandong Focus Biotechnology 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]Zhejiang Huakang Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Topical
Emulsifying Agents
Thickeners and Stabilizers
Controlled & Modified Release
Surfactant & Foaming Agents
Chewable & Orodispersible Aids
Coating Systems & Additives
Fillers, Diluents & Binders
Parenteral
Taste Masking
API Stability Enhancers
Direct Compression
Rheology Modifiers
Lubricants & Glidants
Disintegrants & Superdisintegrants
Film Formers & Plasticizers
Co-Processed Excipients
Market Place
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Sulisobenzone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulisobenzone, including repackagers and relabelers. The FDA regulates Sulisobenzone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulisobenzone API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Sulisobenzone supplier is an individual or a company that provides Sulisobenzone active pharmaceutical ingredient (API) or Sulisobenzone finished formulations upon request. The Sulisobenzone suppliers may include Sulisobenzone API manufacturers, exporters, distributors and traders.
click here to find a list of Sulisobenzone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sulisobenzone DMF (Drug Master File) is a document detailing the whole manufacturing process of Sulisobenzone active pharmaceutical ingredient (API) in detail. Different forms of Sulisobenzone DMFs exist exist since differing nations have different regulations, such as Sulisobenzone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sulisobenzone DMF submitted to regulatory agencies in the US is known as a USDMF. Sulisobenzone USDMF includes data on Sulisobenzone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sulisobenzone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sulisobenzone 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 Sulisobenzone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sulisobenzone 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 Sulisobenzone 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 Sulisobenzone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sulisobenzone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sulisobenzone suppliers with NDC on PharmaCompass.
Sulisobenzone 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 Sulisobenzone 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 Sulisobenzone GMP manufacturer or Sulisobenzone GMP API supplier for your needs.
A Sulisobenzone CoA (Certificate of Analysis) is a formal document that attests to Sulisobenzone's compliance with Sulisobenzone specifications and serves as a tool for batch-level quality control.
Sulisobenzone CoA mostly includes findings from lab analyses of a specific batch. For each Sulisobenzone 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.
Sulisobenzone may be tested according to a variety of international standards, such as European Pharmacopoeia (Sulisobenzone EP), Sulisobenzone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sulisobenzone USP).
LOOKING FOR A SUPPLIER?
