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  • TABLET;ORAL - 1MG
  • TABLET;ORAL - 2MG
  • CAPSULE, EXTENDED RELEASE;ORAL - 2MG
  • CAPSULE, EXTENDED RELEASE;ORAL - 4MG

Looking for 124937-52-6 / Tolterodine Tartrate API manufacturers, exporters & distributors?

Tolterodine Tartrate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Tolterodine Tartrate

Synonyms

124937-52-6, Detrol la, Detrusitol, Tolterodine l-tartrate, Pnu-200583e, (r)-2-(3-(diisopropylamino)-1-phenylpropyl)-4-methylphenol (2r,3r)-2,3-dihydroxysuccinate

Cas Number

124937-52-6

Unique Ingredient Identifier (UNII)

5T619TQR3R

About Tolterodine Tartrate

An ANTIMUSCARINIC AGENT selective for the MUSCARINIC RECEPTORS of the BLADDER that is used in the treatment of URINARY INCONTINENCE and URINARY URGE INCONTINENCE.

tolterodine, tartrate Manufacturers

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

tolterodine, tartrate Suppliers

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

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

tolterodine, tartrate USDMF

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

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

click here to find a list of tolterodine, tartrate suppliers with USDMF on PharmaCompass.

tolterodine, tartrate KDMF

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

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

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

click here to find a list of tolterodine, tartrate suppliers with KDMF on PharmaCompass.

tolterodine, tartrate CEP

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

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

tolterodine, tartrate WC

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

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

tolterodine, tartrate 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 tolterodine, tartrate as an active pharmaceutical ingredient (API).

Finished drug products

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

click here to find a list of tolterodine, tartrate suppliers with NDC on PharmaCompass.

tolterodine, tartrate GMP

tolterodine, tartrate 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 tolterodine, tartrate 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 tolterodine, tartrate GMP manufacturer or tolterodine, tartrate GMP API supplier for your needs.

tolterodine, tartrate CoA

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

tolterodine, tartrate CoA mostly includes findings from lab analyses of a specific batch. For each tolterodine, tartrate 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.

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