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Looking for 537-55-3 / N-Acetyl-L-Tyrosine API manufacturers, exporters & distributors?

N-Acetyl-L-Tyrosine manufacturers, exporters & distributors 1

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PharmaCompass offers a list of N-Acetyl-L-Tyrosine 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 N-Acetyl-L-Tyrosine manufacturer or N-Acetyl-L-Tyrosine supplier for your needs.

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

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

API | Excipient name

N-Acetyl-L-Tyrosine

Synonyms

537-55-3, Ac-tyr-oh, N-acetyl-tyrosine, Acetyl tyrosine, Acetyl-l-tyrosine, L-tyrosine, n-acetyl-

Cas Number

537-55-3

Unique Ingredient Identifier (UNII)

DA8G610ZO5

About N-Acetyl-L-Tyrosine

N-acetyltyrosine, also referred to as N-acetyl-L-tyrosine, is used in place of as a tyrosine precursor. [DB00135] is a non-essential amino acid with a polar side group. N-acetyltyrosine is administered as parenteral nutrition or intravenous infusion due to its enhanced solubility compared to tyrosine. It is typically administered as a source of nutritional support where oral nutrition is inadequate or cannot be tolerated.

MolPort-001-792-339 Manufacturers

A MolPort-001-792-339 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-792-339, including repackagers and relabelers. The FDA regulates MolPort-001-792-339 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-792-339 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-001-792-339 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-001-792-339 Suppliers

A MolPort-001-792-339 supplier is an individual or a company that provides MolPort-001-792-339 active pharmaceutical ingredient (API) or MolPort-001-792-339 finished formulations upon request. The MolPort-001-792-339 suppliers may include MolPort-001-792-339 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-001-792-339 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-001-792-339 USDMF

A MolPort-001-792-339 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-792-339 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-792-339 DMFs exist exist since differing nations have different regulations, such as MolPort-001-792-339 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A MolPort-001-792-339 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-792-339 USDMF includes data on MolPort-001-792-339's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-792-339 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of MolPort-001-792-339 suppliers with USDMF on PharmaCompass.

MolPort-001-792-339 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 MolPort-001-792-339 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for MolPort-001-792-339 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 MolPort-001-792-339 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 MolPort-001-792-339 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MolPort-001-792-339 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of MolPort-001-792-339 suppliers with NDC on PharmaCompass.

MolPort-001-792-339 GMP

MolPort-001-792-339 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-001-792-339 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-001-792-339 GMP manufacturer or MolPort-001-792-339 GMP API supplier for your needs.

MolPort-001-792-339 CoA

A MolPort-001-792-339 CoA (Certificate of Analysis) is a formal document that attests to MolPort-001-792-339's compliance with MolPort-001-792-339 specifications and serves as a tool for batch-level quality control.

MolPort-001-792-339 CoA mostly includes findings from lab analyses of a specific batch. For each MolPort-001-792-339 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-001-792-339 may be tested according to a variety of international standards, such as European Pharmacopoeia (MolPort-001-792-339 EP), MolPort-001-792-339 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MolPort-001-792-339 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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