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Looking for 7429-90-5 / Aluminum API manufacturers, exporters & distributors?

Aluminum manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Aluminum

Synonyms

7429-90-5, Al, Aluminium, Aluminum metal, Aluminum powder, Bts-catalyst

Cas Number

7429-90-5

Unique Ingredient Identifier (UNII)

KZJ3T010RQ

About Aluminum

Inorganic compounds that contain aluminum as an integral part of the molecule.

Aluminum, molten Manufacturers

A Aluminum, molten manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aluminum, molten, including repackagers and relabelers. The FDA regulates Aluminum, molten manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aluminum, molten API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Aluminum, molten Suppliers

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

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

Aluminum, molten CEP

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

A Aluminum, molten CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aluminum, molten 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, molten suppliers with CEP (COS) on PharmaCompass.

Aluminum, molten 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, molten as an active pharmaceutical ingredient (API).

Finished drug products

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

click here to find a list of Aluminum, molten suppliers with NDC on PharmaCompass.

Aluminum, molten GMP

Aluminum, molten 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, molten 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, molten GMP manufacturer or Aluminum, molten GMP API supplier for your needs.

Aluminum, molten CoA

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

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