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API SUPPLIERS
Dr. Paul Lohmann® provides premium mineral salts backed by 140+ years of innovation, quality manufacturing, and global expertise.
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USDMF
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Dr. Paul Lohmann® provides premium mineral salts backed by 140+ years of innovation, quality manufacturing, and global expertise.
About the Company : Dr. Paul Lohmann® is a Germany based developer & manufacturer of high quality mineral salts with over 140 years of expertise. The company offers more than 400 salts in over 7,000 ...
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EUROAPI
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Rochem International Inc
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]SPI Pharma
SPI Pharma has been solving formulation challenges using superior functional materials.
Dosage Form : Tablet
Grade : Oral
Application : Controlled & Modified Release
Excipient Details : ACTILLETS are microcrystalline cellulose spheres developed using advanced drug delivery technology to enable effective loading & coating of particles.
Pharmacopoeia Ref : NA
Technical Specs : Not Available
Ingredient(s) : Microcrystalline Cellulose Excipients
SPI Pharma has been solving formulation challenges using superior functional materials.
Dosage Form : Tablet
Grade : Oral
SPI Pharma has been solving formulation challenges using superior functional materials.
Dosage Form : Tablet
Grade : Oral
SPI Pharma has been solving formulation challenges using superior functional materials.
Dosage Form : Tablet
Grade : Oral
SPI Pharma has been solving formulation challenges using superior functional materials.
Dosage Form : Tablet
Grade : Oral
Application : Taste Masking
Excipient Details : CS90 is a directly compressible calcium carbonate with starch used for chewable tablets due to its smooth mouthfeel and creamy texture.
Pharmacopoeia Ref : NA
Technical Specs : PSD D50: 150-175 µm, Tapped Density: 0.85
Ingredient(s) : Calcium Carbonate Excipient
SPI Pharma has been solving formulation challenges using superior functional materials.
Dosage Form : Tablet
Grade : Oral
Application : Disintegrants & Superdisintegrants
Excipient Details : Mannogem 2080 exhibits excellent flow, disintegration and compression properties.
SPI Pharma has been solving formulation challenges using superior functional materials.
Dosage Form : Orodispersible Tablet
Grade : Oral
SPI Pharma has been solving formulation challenges using superior functional materials.
Dosage Form : Tablet
Grade : Oral
SPI Pharma has been solving formulation challenges using superior functional materials.
Dosage Form : Tablet
Grade : Oral
SPI Pharma has been solving formulation challenges using superior functional materials.
Dosage Form : Tablet
Grade : Oral
Application : Taste Masking
Excipient Details : MS90 is a directly compressible magnesium hydroxide with starch used for chewable tablets due to its smooth mouthfeel and creamy texture.
Pharmacopoeia Ref : NA
Technical Specs : PSD D50: 150-170 µm, Tapped Density: 0.80
Ingredient(s) : Magnesium Hydroxide Excipient
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Boai NKY Pharmaceuticals Ltd
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
Nanjing Well is focused on R&D, production & sales of Pharmaceutical Excipients & Synthetic Lubricating base oils.
Dosage Form : Softgels
Grade : Oral
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pfanstiehl
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Dr. Paul Lohmann GmbH & Co. KGaA
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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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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Fillers, Diluents & Binders
Direct Compression
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Parenteral
Chewable & Orodispersible Aids
Thickeners and Stabilizers
Film Formers & Plasticizers
Co-Processed Excipients
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Disintegrants & Superdisintegrants
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Coating Systems & Additives
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ABOUT THIS PAGE
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PharmaCompass offers a list of Disodium Carbonate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Disodium Carbonate manufacturer or Disodium Carbonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Disodium Carbonate manufacturer or Disodium Carbonate supplier.
A Natrium Carbonicum Siccatum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Natrium Carbonicum Siccatum, including repackagers and relabelers. The FDA regulates Natrium Carbonicum Siccatum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Natrium Carbonicum Siccatum 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 Natrium Carbonicum Siccatum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Natrium Carbonicum Siccatum supplier is an individual or a company that provides Natrium Carbonicum Siccatum active pharmaceutical ingredient (API) or Natrium Carbonicum Siccatum finished formulations upon request. The Natrium Carbonicum Siccatum suppliers may include Natrium Carbonicum Siccatum API manufacturers, exporters, distributors and traders.
click here to find a list of Natrium Carbonicum Siccatum suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Natrium Carbonicum Siccatum DMF (Drug Master File) is a document detailing the whole manufacturing process of Natrium Carbonicum Siccatum active pharmaceutical ingredient (API) in detail. Different forms of Natrium Carbonicum Siccatum DMFs exist exist since differing nations have different regulations, such as Natrium Carbonicum Siccatum USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Natrium Carbonicum Siccatum DMF submitted to regulatory agencies in the US is known as a USDMF. Natrium Carbonicum Siccatum USDMF includes data on Natrium Carbonicum Siccatum's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Natrium Carbonicum Siccatum USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Natrium Carbonicum Siccatum suppliers with USDMF on PharmaCompass.
A Natrium Carbonicum Siccatum CEP of the European Pharmacopoeia monograph is often referred to as a Natrium Carbonicum Siccatum Certificate of Suitability (COS). The purpose of a Natrium Carbonicum Siccatum CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Natrium Carbonicum Siccatum EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Natrium Carbonicum Siccatum to their clients by showing that a Natrium Carbonicum Siccatum CEP has been issued for it. The manufacturer submits a Natrium Carbonicum Siccatum CEP (COS) as part of the market authorization procedure, and it takes on the role of a Natrium Carbonicum Siccatum CEP holder for the record. Additionally, the data presented in the Natrium Carbonicum Siccatum CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Natrium Carbonicum Siccatum DMF.
A Natrium Carbonicum Siccatum CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Natrium Carbonicum Siccatum 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 Natrium Carbonicum Siccatum suppliers with CEP (COS) on PharmaCompass.
A Natrium Carbonicum Siccatum written confirmation (Natrium Carbonicum Siccatum WC) is an official document issued by a regulatory agency to a Natrium Carbonicum Siccatum manufacturer, verifying that the manufacturing facility of a Natrium Carbonicum Siccatum active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Natrium Carbonicum Siccatum APIs or Natrium Carbonicum Siccatum finished pharmaceutical products to another nation, regulatory agencies frequently require a Natrium Carbonicum Siccatum WC (written confirmation) as part of the regulatory process.
click here to find a list of Natrium Carbonicum Siccatum suppliers with Written Confirmation (WC) on PharmaCompass.
Natrium Carbonicum Siccatum 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 Natrium Carbonicum Siccatum GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Natrium Carbonicum Siccatum GMP manufacturer or Natrium Carbonicum Siccatum GMP API supplier for your needs.
A Natrium Carbonicum Siccatum CoA (Certificate of Analysis) is a formal document that attests to Natrium Carbonicum Siccatum's compliance with Natrium Carbonicum Siccatum specifications and serves as a tool for batch-level quality control.
Natrium Carbonicum Siccatum CoA mostly includes findings from lab analyses of a specific batch. For each Natrium Carbonicum Siccatum 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.
Natrium Carbonicum Siccatum may be tested according to a variety of international standards, such as European Pharmacopoeia (Natrium Carbonicum Siccatum EP), Natrium Carbonicum Siccatum JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Natrium Carbonicum Siccatum USP).
