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1. Dried Aluminum Hydroxide Gel
2. Aluminum;trihydroxide
3. Aluminium Hydroxide Gel, Dried
4. Dried Aluminium Hydroxide
5. Aluminum Hydroxide, Dried
6. Aluminium Hydroxide, Dried
7. Aluminum Hydroxide Gel, Dried
8. Nsc-664400
9. Aluminum Hydrate
10. Aluminum Hyroxide
11. Aluminium Trihydroxide
12. Hydroxyde D' Aluminium
13. Algeldrate Anhydrous
14. Aluminum (as Hydroxide)
15. Aluminum Hydroxide [ii]
16. Aluminum Hydroxide [mi]
17. Chembl1200706
18. Dtxsid2036405
19. Niosh/bd0708000
20. Aluminum Hydroxide [inci]
21. Di-mu-hydroxytetrahydroxydialuminum
22. Aluminum Hydroxide [vandf]
23. Aluminium Hydroxide[who-ip]
24. Aluminum Hydroxide [mart.]
25. Aluminum Hydroxide Gel,dried
26. Aluminium Hydroxide Dried Gel
27. Af-260
28. Aluminium Hydroxide [who-dd]
29. Akos015904617
30. Aluminum, Di-mu-hydroxytetrahydroxydi-
31. Db06723
32. Aluminum Hydroxide [orange Book]
33. Aluminii Hydroxidum[who-ip Latin]
34. Aluminum (as Hydroxide) [vandf]
35. Aluminum Hydroxide [usp Impurity]
36. Aluminum Hydroxide, Dried [hsdb]
37. As04 Component Aluminum Hydroxide
38. Aluminum Hydroxide Gel, Dried [ii]
39. Foamcoat Component Aluminum Hydroxide
40. Foamicon Component Aluminum Hydroxide
41. Gaviscon Component Aluminum Hydroxide
42. Aluminum Hydroxide Gel,dried [vandf]
43. Bd07080000
44. Dried Aluminum Hydroxide Gel [usp-rs]
45. Aluminum Hydroxide Component Of Foamcoat
46. Aluminum Hydroxide Component Of Foamicon
47. Aluminum Hydroxide Component Of Gaviscon
48. Aluminium Hydroxide Gel, Dried [who-dd]
49. Aluminum Hydroxide, Dried [usp Impurity]
50. Q407125
51. J-014205
52. 8012-63-3
Molecular Weight | 78.004 g/mol |
---|---|
Molecular Formula | AlH3O3 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 0 |
Exact Mass | 77.9897574 g/mol |
Monoisotopic Mass | 77.9897574 g/mol |
Topological Polar Surface Area | 3 Ų |
Heavy Atom Count | 4 |
Formal Charge | 0 |
Complexity | 0 |
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 | 4 |
For relief of heartburn and acid indigestion.
Gastric-peptic disease occurs as a result of an imbalance between protective factors, such as mucus, bicarbonate, and prostaglandin secretion, and aggressive factors, such as hydrochloric acid, pepsin, and Helicobacter pylori (H. pylori). Antacids work by restoring acid-base balance, attenuating the pepsin activity and increasing bicarbonate and prostaglandin secretion.
Absorption
Approximately 17-30% of the aluminum chloride formed is absorbed.
Route of Elimination
Absorbed aluminum chloride is rapidly eliminated by the kidneys in patients with normal renal function.
Not metabolized.
Aluminum hydroxide is a basic inorganic salt that acts by neutralizing hydrochloric acid in gastric secretions. Aluminum hydroxide is slowly solubilized in the stomach and reacts with hydrochloric acid to form aluminum chloride and water. It also inhibits the action of pepsin by increasing the pH and via adsorption. Cytoprotective effects may occur through increases in bicarbonate ion (HCO3-) and prostaglandins.
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38885
Submission : 2023-11-18
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38895
Submission : 2023-11-18
Status : Active
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39719
Submission : 2024-04-22
Status : Active
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8222
Submission : 1989-09-20
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21384
Submission : 2008-02-21
Status : Inactive
Type : II
Date of Issue : 2024-06-19
Valid Till : 2027-06-19
Written Confirmation Number : WC-0492
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38885
Submission : 2023-11-18
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38895
Submission : 2023-11-18
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21384
Submission : 2008-02-21
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8222
Submission : 1989-09-20
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39719
Submission : 2024-04-22
Status : Active
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Aluminium Hydroxide Gel USP/ Aluminium Hydroxide IP/BP
Date of Issue : 2024-05-20
Valid Till : 2027-05-20
Written Confirmation Number : WC-0551
Address of the Firm : Plot Nos. 281, Kundaim Industrial Estate, Kundaim, Goa 403115
DRIED ALUMINUM HYDROXIDE (Gel) USP/NF
Date of Issue : 2019-09-11
Valid Till : 2022-09-10
Written Confirmation Number : WC-0452
Address of the Firm : Block No.3 of Plot No. 1296, 1297/08, Ward No. 03, Mouza- Waddhamna, Amravati Ro...
Date of Issue : 2024-06-19
Valid Till : 2027-06-19
Written Confirmation Number : WC-0492
Address of the Firm : 333/1, Phase 11, G.I.D.C Industrial Estate, Chitra, Bhavnagar, Gujarat.
Dried Aluminium Hydroxide (BP)
Date of Issue : 2020-02-24
Valid Till : 2022-07-02
Written Confirmation Number : WC-0187
Address of the Firm : Plot No.133, S. V. Co-Op. Indl. Estate, Bollaram, Medak Dist, AP
Dried Aluminium Hydroxide Gel (USP)
Date of Issue : 2020-02-24
Valid Till : 2022-07-02
Written Confirmation Number : WC-0187
Address of the Firm : Plot No.133, S. V. Co-Op. Indl. Estate, Bollaram, Medak Dist, AP
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
About the Company : Established in 1994, Rochem is a distributor of pharmaceutical, food, nutritional and animal health ingredients to some of the largest companies in the world. It sources high-quali...
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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...
Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
About the Company : Octavius Pharma is a global leader in Directly Compressible Granules with over 40 years of experience in Formulation development, manufacturing and commercialization. It offers a w...
About the Company : ChemiGnition is a specialty pharmaceutical company engaged in development, manufacture and marketing of high-quality, industry-leading Intermediates and Active Pharmaceutical Ingre...
About the Company : Guangzhou Tosun Pharmaceutical was founded in 1999, which mainly focuses on importation & exportation of Active Pharmaceutical Ingrediants, Chemical Raw Materials, Intermediate, Ex...
About the Company : Nitika Pharmaceutical Specialities was found in 1991 as a small manufacturing unit has grown today into a dynamic production center for a range of products finding applications in ...
About the Company : Rumit group of companies is a young, dynamic & Robustly growing company established in 1993. We specialise in pharmaceutical raw material, Bulk API, dye stuff, dyes intermediates &...
About the Company : Sino-Aluminas Ltd, registered in the UK, is the designated sales representative of CHALCO in Europe. The services provided by Sino-Aluminas are to promote alumina chemicals manufac...
API Imports and Exports
Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Aluminium Hydroxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aluminium Hydroxide, including repackagers and relabelers. The FDA regulates Aluminium Hydroxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aluminium Hydroxide 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 Aluminium Hydroxide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aluminium Hydroxide supplier is an individual or a company that provides Aluminium Hydroxide active pharmaceutical ingredient (API) or Aluminium Hydroxide finished formulations upon request. The Aluminium Hydroxide suppliers may include Aluminium Hydroxide API manufacturers, exporters, distributors and traders.
click here to find a list of Aluminium Hydroxide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aluminium Hydroxide DMF (Drug Master File) is a document detailing the whole manufacturing process of Aluminium Hydroxide active pharmaceutical ingredient (API) in detail. Different forms of Aluminium Hydroxide DMFs exist exist since differing nations have different regulations, such as Aluminium Hydroxide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Aluminium Hydroxide DMF submitted to regulatory agencies in the US is known as a USDMF. Aluminium Hydroxide USDMF includes data on Aluminium Hydroxide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Aluminium Hydroxide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Aluminium Hydroxide suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Aluminium Hydroxide Drug Master File in Japan (Aluminium Hydroxide JDMF) empowers Aluminium Hydroxide API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Aluminium Hydroxide JDMF during the approval evaluation for pharmaceutical products. At the time of Aluminium Hydroxide JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Aluminium Hydroxide suppliers with JDMF on PharmaCompass.
A Aluminium Hydroxide written confirmation (Aluminium Hydroxide WC) is an official document issued by a regulatory agency to a Aluminium Hydroxide manufacturer, verifying that the manufacturing facility of a Aluminium Hydroxide active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Aluminium Hydroxide APIs or Aluminium Hydroxide finished pharmaceutical products to another nation, regulatory agencies frequently require a Aluminium Hydroxide WC (written confirmation) as part of the regulatory process.
click here to find a list of Aluminium Hydroxide 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 Aluminium Hydroxide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Aluminium Hydroxide 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 Aluminium Hydroxide 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 Aluminium Hydroxide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Aluminium Hydroxide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Aluminium Hydroxide suppliers with NDC on PharmaCompass.
Aluminium Hydroxide 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 Aluminium Hydroxide 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 Aluminium Hydroxide GMP manufacturer or Aluminium Hydroxide GMP API supplier for your needs.
A Aluminium Hydroxide CoA (Certificate of Analysis) is a formal document that attests to Aluminium Hydroxide's compliance with Aluminium Hydroxide specifications and serves as a tool for batch-level quality control.
Aluminium Hydroxide CoA mostly includes findings from lab analyses of a specific batch. For each Aluminium Hydroxide 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.
Aluminium Hydroxide may be tested according to a variety of international standards, such as European Pharmacopoeia (Aluminium Hydroxide EP), Aluminium Hydroxide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Aluminium Hydroxide USP).
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