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Looking for 645-05-6 / Altretamine API manufacturers, exporters & distributors?

Altretamine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Altretamine

Synonyms

645-05-6, Hexamethylmelamine, Hexalen, Hexastat, Hemel, 2,4,6-tris(dimethylamino)-1,3,5-triazine

Cas Number

645-05-6

Unique Ingredient Identifier (UNII)

Q8BIH59O7H

About Altretamine

A hexamethyl-2,4,6-triamine derivative of 1,3,5-triazine.

Altretamin Manufacturers

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

Altretamin Suppliers

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

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

Altretamin USDMF

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

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

click here to find a list of Altretamin suppliers with USDMF on PharmaCompass.

Altretamin GMP

Altretamin 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 Altretamin 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 Altretamin GMP manufacturer or Altretamin GMP API supplier for your needs.

Altretamin CoA

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

Altretamin CoA mostly includes findings from lab analyses of a specific batch. For each Altretamin 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.

Altretamin may be tested according to a variety of international standards, such as European Pharmacopoeia (Altretamin EP), Altretamin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Altretamin 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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