Synopsis
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CEP/COS
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JDMF
0
EU WC
0
KDMF
0
VMF
0
EDQM
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USP
0
JP
0
Others
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FDA Orange Book
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Europe
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Canada
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Australia
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
US Medicaid
NA
Annual Reports
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Regulatory FDF Prices
NA
0
FDF
0
Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
API SUPPLIERS
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
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USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]NDC API
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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]South Africa
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
EUROAPI
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Dosage Form : Tablet
Grade : Oral
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Dosage Form : Cream / Lotion / Ointment
Grade : Topical, Parenteral
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Rochem International Inc
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Dosage Form : Suspension
Grade : Oral
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Dosage Form : Capsule
Grade : Topical, Oral
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Dosage Form : Cream / Lotion / Ointment
Grade : Topical, Oral
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Dosage Form : Suspension
Grade : Oral
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Dosage Form : Tablet
Grade : Oral
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Dosage Form : Suspension
Grade : Oral
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Dosage Form : Cream / Lotion / Ointment
Grade : Topical
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Dosage Form : Capsule
Grade : Oral
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]DKSH
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Suspension
Grade : Oral
Application : Rheology Modifiers
Excipient Details : Blanose CMC 7MF is used as a thickener and viscosity modifier in liquid formulations such as suspensions.
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Suspension
Grade : Oral
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Suspension
Grade : Oral
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Suspension
Grade : Oral
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Tablet
Grade : Oral
Application : Emulsifying Agents
Excipient Details : HDK N20 Pharma is used as a pharmaceutical emulsifying agent in tablets, capsules, syrups, and solutions.
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Syrup
Grade : Oral
Application : Taste Masking
Excipient Details : Insoluble saccharin (Q-0350, 15-191201) is used as an artificial sweetener in syrups, liquids, suspensions, mouthwashes, and tablets.
Pharmacopoeia Ref : USP/NF, JP, Kosher, ISO, Halal...
Technical Specs : Min. 98% Purity
Ingredient(s) : Saccharin Excipient
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Suspension
Grade : Topical
Application : Rheology Modifiers
Excipient Details : Silfoam® SE 2 is used as a thickener and a viscosity modifier in liquid and topical dosage forms.
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Syrup
Grade : Oral
Application : Taste Masking
Excipient Details : Sodium Saccharin (Q-0300, 15-191201) is used as an artificial sweetener in tablets, syrup, suspensions, liquids, and mouthwashes.
Pharmacopoeia Ref : USP/NF, JP, Kosher, ISO, Halal...
Technical Specs : 15% MOISTURE, Min. 98% Purity
Ingredient(s) : Sodium Saccharin Excipient
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Emulsion
Grade : Topical
Application : Topical
Excipient Details : Triethanolamine is widely used in topical pharmaceutical formulations primarily in the formation of emulsions and sunscreen.
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Suspension
Grade : Topical, Oral
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]Nanjing Well Pharmaceutical
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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]Ashland
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]BASF
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Chemicals
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Lubrizol Life Science Health
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nanjing Bold Chemical
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Prachin Chemical
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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
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ABOUT THIS PAGE
85
PharmaCompass offers a list of Tin Fluoride 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 Tin Fluoride manufacturer or Tin Fluoride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tin Fluoride manufacturer or Tin Fluoride supplier.
PharmaCompass also assists you with knowing the Tin Fluoride API Price utilized in the formulation of products. Tin Fluoride API Price is not always fixed or binding as the Tin Fluoride Price is obtained through a variety of data sources. The Tin Fluoride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Stannous Fluoride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Stannous Fluoride, including repackagers and relabelers. The FDA regulates Stannous Fluoride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Stannous Fluoride 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 Stannous Fluoride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Stannous Fluoride supplier is an individual or a company that provides Stannous Fluoride active pharmaceutical ingredient (API) or Stannous Fluoride finished formulations upon request. The Stannous Fluoride suppliers may include Stannous Fluoride API manufacturers, exporters, distributors and traders.
click here to find a list of Stannous Fluoride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Stannous Fluoride DMF (Drug Master File) is a document detailing the whole manufacturing process of Stannous Fluoride active pharmaceutical ingredient (API) in detail. Different forms of Stannous Fluoride DMFs exist exist since differing nations have different regulations, such as Stannous Fluoride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Stannous Fluoride DMF submitted to regulatory agencies in the US is known as a USDMF. Stannous Fluoride USDMF includes data on Stannous Fluoride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Stannous Fluoride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Stannous Fluoride 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 Stannous Fluoride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Stannous Fluoride 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 Stannous Fluoride 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 Stannous Fluoride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Stannous Fluoride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Stannous Fluoride suppliers with NDC on PharmaCompass.
Stannous Fluoride 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 Stannous Fluoride 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 Stannous Fluoride GMP manufacturer or Stannous Fluoride GMP API supplier for your needs.
A Stannous Fluoride CoA (Certificate of Analysis) is a formal document that attests to Stannous Fluoride's compliance with Stannous Fluoride specifications and serves as a tool for batch-level quality control.
Stannous Fluoride CoA mostly includes findings from lab analyses of a specific batch. For each Stannous Fluoride 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.
Stannous Fluoride may be tested according to a variety of international standards, such as European Pharmacopoeia (Stannous Fluoride EP), Stannous Fluoride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Stannous Fluoride USP).
