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API SUPPLIERS
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Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
About the Company : Pharm-Rx has earned an outstanding reputation since its establishment in 1991, serving as a reputable importer and distributor of active ingredients to the pharmaceutical, nutritio...
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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]Minakem
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DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Suspension
Grade : Oral
Application : Thickeners and Stabilizers
Excipient Details : Blanose CMC 7MF is used as a thickener and viscosity modifier in liquid formulations such as suspensions.
Pharmacopoeia Ref : EP, USP/NF
Technical Specs : N/A
Ingredient(s) : Sodium Carboxymethyl Cellulose Excipient
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Cream / Lotion / Ointment
Grade : Topical
Application : Topical
Excipient Details : Boric acid is used as an antimicrobial preservative in topical formulations such as creams and ointments.
Pharmacopoeia Ref : EP
Technical Specs : 99.9 % Boric Acid (H3BO3)
Ingredient(s) : Boric Acid Excipient
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Injectable / Parenteral
Grade : Parenteral, 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 : Suspension
Grade : Oral, Topical
Application : Rheology Modifiers
Excipient Details : HPMC 60HD4000 is used as thickener and viscosity modifier in oral solid, liquid and topical dosage forms.
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Cream / Lotion / Ointment
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 : Ophthalmic Solution
Grade : Topical, Parenteral
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
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PharmaCompass offers a list of Benzalkonium Chloride 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 Benzalkonium Chloride manufacturer or Benzalkonium Chloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benzalkonium Chloride manufacturer or Benzalkonium Chloride supplier.
PharmaCompass also assists you with knowing the Benzalkonium Chloride API Price utilized in the formulation of products. Benzalkonium Chloride API Price is not always fixed or binding as the Benzalkonium Chloride Price is obtained through a variety of data sources. The Benzalkonium Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Benzyldimethyldodecylammonium Chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benzyldimethyldodecylammonium Chloride, including repackagers and relabelers. The FDA regulates Benzyldimethyldodecylammonium Chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benzyldimethyldodecylammonium Chloride 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 Benzyldimethyldodecylammonium Chloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Benzyldimethyldodecylammonium Chloride supplier is an individual or a company that provides Benzyldimethyldodecylammonium Chloride active pharmaceutical ingredient (API) or Benzyldimethyldodecylammonium Chloride finished formulations upon request. The Benzyldimethyldodecylammonium Chloride suppliers may include Benzyldimethyldodecylammonium Chloride API manufacturers, exporters, distributors and traders.
click here to find a list of Benzyldimethyldodecylammonium Chloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Benzyldimethyldodecylammonium Chloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Benzyldimethyldodecylammonium Chloride active pharmaceutical ingredient (API) in detail. Different forms of Benzyldimethyldodecylammonium Chloride DMFs exist exist since differing nations have different regulations, such as Benzyldimethyldodecylammonium Chloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Benzyldimethyldodecylammonium Chloride DMF submitted to regulatory agencies in the US is known as a USDMF. Benzyldimethyldodecylammonium Chloride USDMF includes data on Benzyldimethyldodecylammonium Chloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Benzyldimethyldodecylammonium Chloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Benzyldimethyldodecylammonium Chloride suppliers with USDMF on PharmaCompass.
A Benzyldimethyldodecylammonium Chloride written confirmation (Benzyldimethyldodecylammonium Chloride WC) is an official document issued by a regulatory agency to a Benzyldimethyldodecylammonium Chloride manufacturer, verifying that the manufacturing facility of a Benzyldimethyldodecylammonium Chloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Benzyldimethyldodecylammonium Chloride APIs or Benzyldimethyldodecylammonium Chloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Benzyldimethyldodecylammonium Chloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Benzyldimethyldodecylammonium Chloride suppliers with Written Confirmation (WC) on PharmaCompass.
Benzyldimethyldodecylammonium Chloride 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 Benzyldimethyldodecylammonium Chloride 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 Benzyldimethyldodecylammonium Chloride GMP manufacturer or Benzyldimethyldodecylammonium Chloride GMP API supplier for your needs.
A Benzyldimethyldodecylammonium Chloride CoA (Certificate of Analysis) is a formal document that attests to Benzyldimethyldodecylammonium Chloride's compliance with Benzyldimethyldodecylammonium Chloride specifications and serves as a tool for batch-level quality control.
Benzyldimethyldodecylammonium Chloride CoA mostly includes findings from lab analyses of a specific batch. For each Benzyldimethyldodecylammonium Chloride 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.
Benzyldimethyldodecylammonium Chloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Benzyldimethyldodecylammonium Chloride EP), Benzyldimethyldodecylammonium Chloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Benzyldimethyldodecylammonium Chloride USP).
