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Looking for 637-12-7 / Aluminum stearate API manufacturers, exporters & distributors?

Aluminum stearate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Aluminum stearate

Synonyms

Aluminium stearate, 637-12-7, Aluminium tristearate, Aluminum octadecanoate, Aluminum tristearate, Octadecanoic acid, aluminum salt

Cas Number

637-12-7

Unique Ingredient Identifier (UNII)

U6XF9NP8HM

About Aluminum stearate

Aluminum Stearate is the aluminum salt of the fatty acid, stearic acid.

Aluminum(III) stearate Manufacturers

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

Aluminum(III) stearate Suppliers

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

click here to find a list of Aluminum(III) stearate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Aluminum(III) stearate USDMF

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

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

click here to find a list of Aluminum(III) stearate suppliers with USDMF on PharmaCompass.

Aluminum(III) stearate CEP

A Aluminum(III) stearate CEP of the European Pharmacopoeia monograph is often referred to as a Aluminum(III) stearate Certificate of Suitability (COS). The purpose of a Aluminum(III) stearate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aluminum(III) stearate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aluminum(III) stearate to their clients by showing that a Aluminum(III) stearate CEP has been issued for it. The manufacturer submits a Aluminum(III) stearate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aluminum(III) stearate CEP holder for the record. Additionally, the data presented in the Aluminum(III) stearate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aluminum(III) stearate DMF.

A Aluminum(III) stearate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aluminum(III) stearate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of Aluminum(III) stearate suppliers with CEP (COS) on PharmaCompass.

Aluminum(III) stearate GMP

Aluminum(III) stearate 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(III) stearate 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(III) stearate GMP manufacturer or Aluminum(III) stearate GMP API supplier for your needs.

Aluminum(III) stearate CoA

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

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