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Looking for 63-91-2 / Phenylalanine API manufacturers, exporters & distributors?

Phenylalanine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Phenylalanine

Synonyms

L-phenylalanine, 63-91-2, 3-phenyl-l-alanine, (2s)-2-amino-3-phenylpropanoic acid, (s)-2-amino-3-phenylpropanoic acid, (s)-phenylalanine

Cas Number

63-91-2

Unique Ingredient Identifier (UNII)

47E5O17Y3R

About Phenylalanine

An essential aromatic amino acid that is a precursor of MELANIN; DOPAMINE; noradrenalin (NOREPINEPHRINE), and THYROXINE.

MolPort-001-757-101 Manufacturers

A MolPort-001-757-101 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-757-101, including repackagers and relabelers. The FDA regulates MolPort-001-757-101 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-757-101 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-001-757-101 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-001-757-101 Suppliers

A MolPort-001-757-101 supplier is an individual or a company that provides MolPort-001-757-101 active pharmaceutical ingredient (API) or MolPort-001-757-101 finished formulations upon request. The MolPort-001-757-101 suppliers may include MolPort-001-757-101 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-001-757-101 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-001-757-101 USDMF

A MolPort-001-757-101 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-757-101 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-757-101 DMFs exist exist since differing nations have different regulations, such as MolPort-001-757-101 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A MolPort-001-757-101 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-757-101 USDMF includes data on MolPort-001-757-101's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-757-101 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of MolPort-001-757-101 suppliers with USDMF on PharmaCompass.

MolPort-001-757-101 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 MolPort-001-757-101 Drug Master File in Japan (MolPort-001-757-101 JDMF) empowers MolPort-001-757-101 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 MolPort-001-757-101 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-001-757-101 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 MolPort-001-757-101 suppliers with JDMF on PharmaCompass.

MolPort-001-757-101 CEP

A MolPort-001-757-101 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-001-757-101 Certificate of Suitability (COS). The purpose of a MolPort-001-757-101 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-001-757-101 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-001-757-101 to their clients by showing that a MolPort-001-757-101 CEP has been issued for it. The manufacturer submits a MolPort-001-757-101 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-001-757-101 CEP holder for the record. Additionally, the data presented in the MolPort-001-757-101 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-001-757-101 DMF.

A MolPort-001-757-101 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-001-757-101 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 MolPort-001-757-101 suppliers with CEP (COS) on PharmaCompass.

MolPort-001-757-101 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-001-757-101 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for MolPort-001-757-101 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-001-757-101 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-001-757-101 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MolPort-001-757-101 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of MolPort-001-757-101 suppliers with NDC on PharmaCompass.

MolPort-001-757-101 GMP

MolPort-001-757-101 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-001-757-101 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-001-757-101 GMP manufacturer or MolPort-001-757-101 GMP API supplier for your needs.

MolPort-001-757-101 CoA

A MolPort-001-757-101 CoA (Certificate of Analysis) is a formal document that attests to MolPort-001-757-101's compliance with MolPort-001-757-101 specifications and serves as a tool for batch-level quality control.

MolPort-001-757-101 CoA mostly includes findings from lab analyses of a specific batch. For each MolPort-001-757-101 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-001-757-101 may be tested according to a variety of international standards, such as European Pharmacopoeia (MolPort-001-757-101 EP), MolPort-001-757-101 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MolPort-001-757-101 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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