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  • TABLET;ORAL - EQ 0.005MG BASE
  • TABLET;ORAL - EQ 0.025MG BASE
  • TABLET;ORAL - EQ 0.05MG BASE
  • INJECTABLE;INJECTION - EQ 0.01MG BASE/ML

Looking for 55-06-1 / Liothyronine Sodium API manufacturers, exporters & distributors?

Liothyronine Sodium manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Liothyronine Sodium

Synonyms

55-06-1, Cytomel, Triostat, 3,3',5-triiodo-l-thyronine sodium salt, Tertroxin, T3 sodium salt

Cas Number

55-06-1

Unique Ingredient Identifier (UNII)

GCA9VV7D2N

About Liothyronine Sodium

A T3 thyroid hormone normally synthesized and secreted by the thyroid gland in much smaller quantities than thyroxine (T4). Most T3 is derived from peripheral monodeiodination of T4 at the 5' position of the outer ring of the iodothyronine nucleus. The hormone finally delivered and used by the tissues is mainly T3.

Triiodothyronine Manufacturers

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

Triiodothyronine Suppliers

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

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

Triiodothyronine USDMF

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

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

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

Triiodothyronine JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The Triiodothyronine Drug Master File in Japan (Triiodothyronine JDMF) empowers Triiodothyronine API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the Triiodothyronine JDMF during the approval evaluation for pharmaceutical products. At the time of Triiodothyronine JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of Triiodothyronine suppliers with JDMF on PharmaCompass.

Triiodothyronine KDMF

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

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

After submitting a Triiodothyronine 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 Triiodothyronine API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Triiodothyronine suppliers with KDMF on PharmaCompass.

Triiodothyronine CEP

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

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

Triiodothyronine WC

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

click here to find a list of Triiodothyronine suppliers with Written Confirmation (WC) on PharmaCompass.

Triiodothyronine 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 Triiodothyronine as an active pharmaceutical ingredient (API).

Finished drug products

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

click here to find a list of Triiodothyronine suppliers with NDC on PharmaCompass.

Triiodothyronine GMP

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

Triiodothyronine CoA

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

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

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