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Looking for 1317-26-6 / Magaldrate API manufacturers, exporters & distributors?

Magaldrate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Magaldrate

Synonyms

1317-26-6, Aluminum hydroxide/magnesium hydroxide, Aluminum hydroxide/magnesium hydroxide - magaldrate c410, Aluminum hydroxide/magnesium hydroxide - magaldrate c632

Cas Number

1317-26-6

About Magaldrate

Aluminum Hydroxide/Magnesium Hydroxide is an oral suspension containing aluminum hydroxide and magnesium hydroxide, with antacid effects. Aluminum hydroxide and magnesium hydroxide neutralizes or reduces gastric acid, thereby relieving symptoms associated with indigestion, gastritis, and gastroesophageal disease (GERD). Combined with other liquid ingredients (such as lidocaine and diphenhydramine), this antacid provides relief for painful stomatitis, mucositis, and esophagitis associated with both chemotherapy and radiation therapy.

Aluminum Magnesium Hydroxide Monohydrate Manufacturers

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

Aluminum Magnesium Hydroxide Monohydrate Suppliers

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

click here to find a list of Aluminum Magnesium Hydroxide Monohydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Aluminum Magnesium Hydroxide Monohydrate USDMF

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

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

click here to find a list of Aluminum Magnesium Hydroxide Monohydrate suppliers with USDMF on PharmaCompass.

Aluminum Magnesium Hydroxide Monohydrate WC

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

click here to find a list of Aluminum Magnesium Hydroxide Monohydrate suppliers with Written Confirmation (WC) on PharmaCompass.

Aluminum Magnesium Hydroxide Monohydrate 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 Magnesium Hydroxide Monohydrate as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Aluminum Magnesium Hydroxide Monohydrate 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 Magnesium Hydroxide Monohydrate 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 Magnesium Hydroxide Monohydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Aluminum Magnesium Hydroxide Monohydrate NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Aluminum Magnesium Hydroxide Monohydrate suppliers with NDC on PharmaCompass.

Aluminum Magnesium Hydroxide Monohydrate GMP

Aluminum Magnesium Hydroxide Monohydrate 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 Magnesium Hydroxide Monohydrate 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 Magnesium Hydroxide Monohydrate GMP manufacturer or Aluminum Magnesium Hydroxide Monohydrate GMP API supplier for your needs.

Aluminum Magnesium Hydroxide Monohydrate CoA

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

Aluminum Magnesium Hydroxide Monohydrate CoA mostly includes findings from lab analyses of a specific batch. For each Aluminum Magnesium Hydroxide Monohydrate 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 Magnesium Hydroxide Monohydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Aluminum Magnesium Hydroxide Monohydrate EP), Aluminum Magnesium Hydroxide Monohydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Aluminum Magnesium Hydroxide Monohydrate 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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