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EUROAPI
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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
Application : Taste Masking
Excipient Details : CM90 is a directly compressible, granulated calcium carbonate with maltodextrin used for swallow tablets due to its high density and compressibility.
Pharmacopoeia Ref : NA
Technical Specs : PSD D50: 490- 500 µm; Tapped Density: 1.50
Ingredient(s) : Calcium Carbonate Excipient
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 : Direct Compression
Excipient Details : DC SIM 100 is a directly compressible simethicone powder used for antacid and anti-gas tablets.
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 : 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
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ABOUT THIS PAGE
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PharmaCompass offers a list of Calcium Phosphate 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 Calcium Phosphate manufacturer or Calcium Phosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcium Phosphate manufacturer or Calcium Phosphate supplier.
PharmaCompass also assists you with knowing the Calcium Phosphate API Price utilized in the formulation of products. Calcium Phosphate API Price is not always fixed or binding as the Calcium Phosphate Price is obtained through a variety of data sources. The Calcium Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tricalcium phosphate hydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tricalcium phosphate hydrate, including repackagers and relabelers. The FDA regulates Tricalcium phosphate hydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tricalcium phosphate hydrate 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 Tricalcium phosphate hydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tricalcium phosphate hydrate supplier is an individual or a company that provides Tricalcium phosphate hydrate active pharmaceutical ingredient (API) or Tricalcium phosphate hydrate finished formulations upon request. The Tricalcium phosphate hydrate suppliers may include Tricalcium phosphate hydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Tricalcium phosphate hydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tricalcium phosphate hydrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Tricalcium phosphate hydrate active pharmaceutical ingredient (API) in detail. Different forms of Tricalcium phosphate hydrate DMFs exist exist since differing nations have different regulations, such as Tricalcium phosphate hydrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tricalcium phosphate hydrate DMF submitted to regulatory agencies in the US is known as a USDMF. Tricalcium phosphate hydrate USDMF includes data on Tricalcium phosphate hydrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tricalcium phosphate hydrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tricalcium phosphate hydrate 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 Tricalcium phosphate hydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tricalcium phosphate hydrate 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 Tricalcium phosphate hydrate 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 Tricalcium phosphate hydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tricalcium phosphate hydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tricalcium phosphate hydrate suppliers with NDC on PharmaCompass.
Tricalcium phosphate hydrate 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 Tricalcium phosphate hydrate 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 Tricalcium phosphate hydrate GMP manufacturer or Tricalcium phosphate hydrate GMP API supplier for your needs.
A Tricalcium phosphate hydrate CoA (Certificate of Analysis) is a formal document that attests to Tricalcium phosphate hydrate's compliance with Tricalcium phosphate hydrate specifications and serves as a tool for batch-level quality control.
Tricalcium phosphate hydrate CoA mostly includes findings from lab analyses of a specific batch. For each Tricalcium phosphate hydrate 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.
Tricalcium phosphate hydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Tricalcium phosphate hydrate EP), Tricalcium phosphate hydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tricalcium phosphate hydrate USP).
