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1. Alginate - Aluminium Hydroxide - Magnesium Trisilicate - Sodium Bicarbonate
2. Alginate, Aluminium Hydroxide, Magnesium Trisilicate, Sodium Bicarbonate Drug Combination
3. Gastrocote
4. Quigel
1. 66220-44-8
2. Gastrocote
3. Quigel
4. Alginic Acid Compound
5. Aac (combination)
6. Foamcoat
7. Foamicon
8. Alginate, Aluminium Hydroxide, Magnesium Trisilicate, Sodium Bicarbonate Drug Combination
9. Alginic Acid, Mixt. With Aluminum Hydroxide, Silicic Acid (h4si3o8) Magnesium Salt (1:2) And Sodium Hydrogen Carbonate
10. Aluminum Hydroxide And Magnesium Trisilicate
| Molecular Weight | 230.40 g/mol |
|---|---|
| Molecular Formula | CH4AlMgNaO7Si |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 0 |
| Exact Mass | 229.9289784 g/mol |
| Monoisotopic Mass | 229.9289784 g/mol |
| Topological Polar Surface Area | 64.4 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 24.8 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 9 |
Antacids
Substances that counteract or neutralize acidity of the GASTROINTESTINAL TRACT. (See all compounds classified as Antacids.)
ABOUT THIS PAGE
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PharmaCompass offers a list of Gastrocote 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 Gastrocote manufacturer or Gastrocote supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gastrocote manufacturer or Gastrocote supplier.
PharmaCompass also assists you with knowing the Gastrocote API Price utilized in the formulation of products. Gastrocote API Price is not always fixed or binding as the Gastrocote Price is obtained through a variety of data sources. The Gastrocote Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gaviscon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gaviscon, including repackagers and relabelers. The FDA regulates Gaviscon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gaviscon API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Gaviscon supplier is an individual or a company that provides Gaviscon active pharmaceutical ingredient (API) or Gaviscon finished formulations upon request. The Gaviscon suppliers may include Gaviscon API manufacturers, exporters, distributors and traders.
Gaviscon 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 Gaviscon 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 Gaviscon GMP manufacturer or Gaviscon GMP API supplier for your needs.
A Gaviscon CoA (Certificate of Analysis) is a formal document that attests to Gaviscon's compliance with Gaviscon specifications and serves as a tool for batch-level quality control.
Gaviscon CoA mostly includes findings from lab analyses of a specific batch. For each Gaviscon 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.
Gaviscon may be tested according to a variety of international standards, such as European Pharmacopoeia (Gaviscon EP), Gaviscon JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Gaviscon USP).
