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Find L-Tyrosine Ethyl Ester Hydrochloride manufacturers, exporters & distributors on PharmaCompass

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Looking for 4089-07-0 / L-Tyrosine Ethyl Ester Hydrochloride API manufacturers, exporters & distributors?

L-Tyrosine Ethyl Ester Hydrochloride manufacturers, exporters & distributors 1

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PharmaCompass offers a list of L-Tyrosine Ethyl Ester Hydrochloride 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 L-Tyrosine Ethyl Ester Hydrochloride manufacturer or L-Tyrosine Ethyl Ester Hydrochloride supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred L-Tyrosine Ethyl Ester Hydrochloride manufacturer or L-Tyrosine Ethyl Ester Hydrochloride supplier.

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

API | Excipient name

L-Tyrosine Ethyl Ester Hydrochloride

Synonyms

4089-07-0, H-tyr-oet.hcl, Ethyl l-tyrosinate hydrochloride, L-tyrosine ethyl ester hcl, (s)-ethyl 2-amino-3-(4-hydroxyphenyl)propanoate hydrochloride, Tyrosine ethyl ester hydrochloride

Cas Number

4089-07-0

Unique Ingredient Identifier (UNII)

FAP58DAZ1E

L-Tyrosine Ethyl Ester Hydrochloride Manufacturers

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

L-Tyrosine Ethyl Ester Hydrochloride Suppliers

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

click here to find a list of L-Tyrosine Ethyl Ester Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

L-Tyrosine Ethyl Ester Hydrochloride USDMF

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

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

click here to find a list of L-Tyrosine Ethyl Ester Hydrochloride suppliers with USDMF on PharmaCompass.

L-Tyrosine Ethyl Ester Hydrochloride 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 L-Tyrosine Ethyl Ester Hydrochloride Drug Master File in Japan (L-Tyrosine Ethyl Ester Hydrochloride JDMF) empowers L-Tyrosine Ethyl Ester Hydrochloride 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 L-Tyrosine Ethyl Ester Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of L-Tyrosine Ethyl Ester Hydrochloride 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 L-Tyrosine Ethyl Ester Hydrochloride suppliers with JDMF on PharmaCompass.

L-Tyrosine Ethyl Ester Hydrochloride GMP

L-Tyrosine Ethyl Ester Hydrochloride 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 L-Tyrosine Ethyl Ester Hydrochloride 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 L-Tyrosine Ethyl Ester Hydrochloride GMP manufacturer or L-Tyrosine Ethyl Ester Hydrochloride GMP API supplier for your needs.

L-Tyrosine Ethyl Ester Hydrochloride CoA

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

L-Tyrosine Ethyl Ester Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each L-Tyrosine Ethyl Ester Hydrochloride 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.

L-Tyrosine Ethyl Ester Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (L-Tyrosine Ethyl Ester Hydrochloride EP), L-Tyrosine Ethyl Ester Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (L-Tyrosine Ethyl Ester Hydrochloride 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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