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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 : Injectable / Parenteral
Grade : Parenteral, Oral
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 : Suspension
Grade : Oral
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 : 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
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Tablet
Grade : Oral
Brand Name : Titanium dioxide PRETIOX ...
Application : Coloring Agents
Excipient Details : Titanium dioxide Pretiox AV01FG is used as a coloring and coating agent in oral solid dosage forms such as capsules, tablets, granules, and pellets.
Pharmacopoeia Ref : Fami-QS, Kosher, Halal, OHSAS ...
Technical Specs : Ti 59.95% and O 40.05%
Ingredient(s) : Titanium Dioxide
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Dosage Form : Tablet
Grade : Oral
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PharmaCompass offers a list of Chromium Picolinate 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 Chromium Picolinate manufacturer or Chromium Picolinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chromium Picolinate manufacturer or Chromium Picolinate supplier.
PharmaCompass also assists you with knowing the Chromium Picolinate API Price utilized in the formulation of products. Chromium Picolinate API Price is not always fixed or binding as the Chromium Picolinate Price is obtained through a variety of data sources. The Chromium Picolinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Chromium Picolinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chromium Picolinate, including repackagers and relabelers. The FDA regulates Chromium Picolinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chromium Picolinate 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 Chromium Picolinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chromium Picolinate supplier is an individual or a company that provides Chromium Picolinate active pharmaceutical ingredient (API) or Chromium Picolinate finished formulations upon request. The Chromium Picolinate suppliers may include Chromium Picolinate API manufacturers, exporters, distributors and traders.
click here to find a list of Chromium Picolinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Chromium Picolinate DMF (Drug Master File) is a document detailing the whole manufacturing process of Chromium Picolinate active pharmaceutical ingredient (API) in detail. Different forms of Chromium Picolinate DMFs exist exist since differing nations have different regulations, such as Chromium Picolinate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Chromium Picolinate DMF submitted to regulatory agencies in the US is known as a USDMF. Chromium Picolinate USDMF includes data on Chromium Picolinate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Chromium Picolinate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Chromium Picolinate suppliers with USDMF on PharmaCompass.
A Chromium Picolinate written confirmation (Chromium Picolinate WC) is an official document issued by a regulatory agency to a Chromium Picolinate manufacturer, verifying that the manufacturing facility of a Chromium Picolinate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Chromium Picolinate APIs or Chromium Picolinate finished pharmaceutical products to another nation, regulatory agencies frequently require a Chromium Picolinate WC (written confirmation) as part of the regulatory process.
click here to find a list of Chromium Picolinate suppliers with Written Confirmation (WC) 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 Chromium Picolinate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Chromium Picolinate 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 Chromium Picolinate 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 Chromium Picolinate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Chromium Picolinate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Chromium Picolinate suppliers with NDC on PharmaCompass.
Chromium Picolinate 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 Chromium Picolinate 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 Chromium Picolinate GMP manufacturer or Chromium Picolinate GMP API supplier for your needs.
A Chromium Picolinate CoA (Certificate of Analysis) is a formal document that attests to Chromium Picolinate's compliance with Chromium Picolinate specifications and serves as a tool for batch-level quality control.
Chromium Picolinate CoA mostly includes findings from lab analyses of a specific batch. For each Chromium Picolinate 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.
Chromium Picolinate may be tested according to a variety of international standards, such as European Pharmacopoeia (Chromium Picolinate EP), Chromium Picolinate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Chromium Picolinate USP).
