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Looking for 77-86-1 / Tromethamine API API manufacturers, exporters & distributors?

Tromethamine API manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Tromethamine API

Synonyms

Trometamol, 77-86-1, Tris(hydroxymethyl)aminomethane, Tris, 2-amino-2-(hydroxymethyl)propane-1,3-diol, Tham

Cas Number

77-86-1

Unique Ingredient Identifier (UNII)

023C2WHX2V

About Tromethamine API

An organic amine proton acceptor. It is used in the synthesis of surface-active agents and pharmaceuticals; as an emulsifying agent for cosmetic creams and lotions, mineral oil and paraffin wax emulsions, as a biological buffer, and used as an alkalizer. (From Merck, 11th ed; Martindale, The Extra Pharmacopoeia, 30th ed, p1424)

MolPort-001-793-006 Manufacturers

A MolPort-001-793-006 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-793-006, including repackagers and relabelers. The FDA regulates MolPort-001-793-006 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-793-006 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 MolPort-001-793-006 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-001-793-006 Suppliers

A MolPort-001-793-006 supplier is an individual or a company that provides MolPort-001-793-006 active pharmaceutical ingredient (API) or MolPort-001-793-006 finished formulations upon request. The MolPort-001-793-006 suppliers may include MolPort-001-793-006 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-001-793-006 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-001-793-006 USDMF

A MolPort-001-793-006 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-793-006 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-793-006 DMFs exist exist since differing nations have different regulations, such as MolPort-001-793-006 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A MolPort-001-793-006 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-793-006 USDMF includes data on MolPort-001-793-006's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-793-006 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of MolPort-001-793-006 suppliers with USDMF on PharmaCompass.

MolPort-001-793-006 KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a MolPort-001-793-006 Drug Master File in Korea (MolPort-001-793-006 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of MolPort-001-793-006. The MFDS reviews the MolPort-001-793-006 KDMF as part of the drug registration process and uses the information provided in the MolPort-001-793-006 KDMF to evaluate the safety and efficacy of the drug.

After submitting a MolPort-001-793-006 KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their MolPort-001-793-006 API can apply through the Korea Drug Master File (KDMF).

click here to find a list of MolPort-001-793-006 suppliers with KDMF on PharmaCompass.

MolPort-001-793-006 GMP

MolPort-001-793-006 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 MolPort-001-793-006 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 MolPort-001-793-006 GMP manufacturer or MolPort-001-793-006 GMP API supplier for your needs.

MolPort-001-793-006 CoA

A MolPort-001-793-006 CoA (Certificate of Analysis) is a formal document that attests to MolPort-001-793-006's compliance with MolPort-001-793-006 specifications and serves as a tool for batch-level quality control.

MolPort-001-793-006 CoA mostly includes findings from lab analyses of a specific batch. For each MolPort-001-793-006 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.

MolPort-001-793-006 may be tested according to a variety of international standards, such as European Pharmacopoeia (MolPort-001-793-006 EP), MolPort-001-793-006 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MolPort-001-793-006 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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