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Looking for 8012-63-3 / Aluminium Hydroxide API manufacturers, exporters & distributors?

Aluminium Hydroxide manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Aluminium Hydroxide 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 Aluminium Hydroxide manufacturer or Aluminium Hydroxide supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aluminium Hydroxide manufacturer or Aluminium Hydroxide supplier.

PharmaCompass also assists you with knowing the Aluminium Hydroxide API Price utilized in the formulation of products. Aluminium Hydroxide API Price is not always fixed or binding as the Aluminium Hydroxide Price is obtained through a variety of data sources. The Aluminium Hydroxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Aluminium Hydroxide

Synonyms

Dried aluminum hydroxide gel, Aluminum;trihydroxide, Aluminium hydroxide gel, dried, Dried aluminium hydroxide, Aluminum hydroxide, dried, Aluminium hydroxide, dried

Cas Number

8012-63-3

Unique Ingredient Identifier (UNII)

5QB0T2IUN0

About Aluminium Hydroxide

Aluminum hydroxide is an inorganic salt used as an antacid. It is a basic compound that acts by neutralizing hydrochloric acid in gastric secretions. Subsequent increases in pH may inhibit the action of pepsin. An increase in bicarbonate ions and prostaglandins may also confer cytoprotective effects.

Aluminum, di-mu-hydroxytetrahydroxydi- Manufacturers

A Aluminum, di-mu-hydroxytetrahydroxydi- manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aluminum, di-mu-hydroxytetrahydroxydi-, including repackagers and relabelers. The FDA regulates Aluminum, di-mu-hydroxytetrahydroxydi- manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aluminum, di-mu-hydroxytetrahydroxydi- 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 Aluminum, di-mu-hydroxytetrahydroxydi- manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Aluminum, di-mu-hydroxytetrahydroxydi- Suppliers

A Aluminum, di-mu-hydroxytetrahydroxydi- supplier is an individual or a company that provides Aluminum, di-mu-hydroxytetrahydroxydi- active pharmaceutical ingredient (API) or Aluminum, di-mu-hydroxytetrahydroxydi- finished formulations upon request. The Aluminum, di-mu-hydroxytetrahydroxydi- suppliers may include Aluminum, di-mu-hydroxytetrahydroxydi- API manufacturers, exporters, distributors and traders.

click here to find a list of Aluminum, di-mu-hydroxytetrahydroxydi- suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Aluminum, di-mu-hydroxytetrahydroxydi- USDMF

A Aluminum, di-mu-hydroxytetrahydroxydi- DMF (Drug Master File) is a document detailing the whole manufacturing process of Aluminum, di-mu-hydroxytetrahydroxydi- active pharmaceutical ingredient (API) in detail. Different forms of Aluminum, di-mu-hydroxytetrahydroxydi- DMFs exist exist since differing nations have different regulations, such as Aluminum, di-mu-hydroxytetrahydroxydi- USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Aluminum, di-mu-hydroxytetrahydroxydi- DMF submitted to regulatory agencies in the US is known as a USDMF. Aluminum, di-mu-hydroxytetrahydroxydi- USDMF includes data on Aluminum, di-mu-hydroxytetrahydroxydi-'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Aluminum, di-mu-hydroxytetrahydroxydi- USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Aluminum, di-mu-hydroxytetrahydroxydi- suppliers with USDMF on PharmaCompass.

Aluminum, di-mu-hydroxytetrahydroxydi- JDMF

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 Aluminum, di-mu-hydroxytetrahydroxydi- Drug Master File in Japan (Aluminum, di-mu-hydroxytetrahydroxydi- JDMF) empowers Aluminum, di-mu-hydroxytetrahydroxydi- 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 Aluminum, di-mu-hydroxytetrahydroxydi- JDMF during the approval evaluation for pharmaceutical products. At the time of Aluminum, di-mu-hydroxytetrahydroxydi- 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 Aluminum, di-mu-hydroxytetrahydroxydi- suppliers with JDMF on PharmaCompass.

Aluminum, di-mu-hydroxytetrahydroxydi- WC

A Aluminum, di-mu-hydroxytetrahydroxydi- written confirmation (Aluminum, di-mu-hydroxytetrahydroxydi- WC) is an official document issued by a regulatory agency to a Aluminum, di-mu-hydroxytetrahydroxydi- manufacturer, verifying that the manufacturing facility of a Aluminum, di-mu-hydroxytetrahydroxydi- active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Aluminum, di-mu-hydroxytetrahydroxydi- APIs or Aluminum, di-mu-hydroxytetrahydroxydi- finished pharmaceutical products to another nation, regulatory agencies frequently require a Aluminum, di-mu-hydroxytetrahydroxydi- WC (written confirmation) as part of the regulatory process.

click here to find a list of Aluminum, di-mu-hydroxytetrahydroxydi- suppliers with Written Confirmation (WC) on PharmaCompass.

Aluminum, di-mu-hydroxytetrahydroxydi- NDC

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 Aluminum, di-mu-hydroxytetrahydroxydi- as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Aluminum, di-mu-hydroxytetrahydroxydi- API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 Aluminum, di-mu-hydroxytetrahydroxydi- 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Aluminum, di-mu-hydroxytetrahydroxydi- and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Aluminum, di-mu-hydroxytetrahydroxydi- NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Aluminum, di-mu-hydroxytetrahydroxydi- suppliers with NDC on PharmaCompass.

Aluminum, di-mu-hydroxytetrahydroxydi- GMP

Aluminum, di-mu-hydroxytetrahydroxydi- 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 Aluminum, di-mu-hydroxytetrahydroxydi- 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 Aluminum, di-mu-hydroxytetrahydroxydi- GMP manufacturer or Aluminum, di-mu-hydroxytetrahydroxydi- GMP API supplier for your needs.

Aluminum, di-mu-hydroxytetrahydroxydi- CoA

A Aluminum, di-mu-hydroxytetrahydroxydi- CoA (Certificate of Analysis) is a formal document that attests to Aluminum, di-mu-hydroxytetrahydroxydi-'s compliance with Aluminum, di-mu-hydroxytetrahydroxydi- specifications and serves as a tool for batch-level quality control.

Aluminum, di-mu-hydroxytetrahydroxydi- CoA mostly includes findings from lab analyses of a specific batch. For each Aluminum, di-mu-hydroxytetrahydroxydi- 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.

Aluminum, di-mu-hydroxytetrahydroxydi- may be tested according to a variety of international standards, such as European Pharmacopoeia (Aluminum, di-mu-hydroxytetrahydroxydi- EP), Aluminum, di-mu-hydroxytetrahydroxydi- JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Aluminum, di-mu-hydroxytetrahydroxydi- USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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