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Looking for 617-65-2 / DL-Glutamic Acid API API manufacturers, exporters & distributors?

DL-Glutamic Acid API manufacturers, exporters & distributors 1

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PharmaCompass offers a list of DL-Glutamic Acid API 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 DL-Glutamic Acid API manufacturer or DL-Glutamic Acid API supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred DL-Glutamic Acid API manufacturer or DL-Glutamic Acid API supplier.

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

API | Excipient name

DL-Glutamic Acid API

Synonyms

617-65-2, 2-aminopentanedioic acid, Glutamic acid, dl-, Glutamic acid dl-form, Glutaminic acid, H-dl-glu-oh

Cas Number

617-65-2

Unique Ingredient Identifier (UNII)

61LJO5I15S

About DL-Glutamic Acid API

A non-essential amino acid naturally occurring in the L-form. Glutamic acid is the most common excitatory neurotransmitter in the CENTRAL NERVOUS SYSTEM.

MolPort-001-779-720 Manufacturers

A MolPort-001-779-720 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-779-720, including repackagers and relabelers. The FDA regulates MolPort-001-779-720 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-779-720 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-001-779-720 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-001-779-720 Suppliers

A MolPort-001-779-720 supplier is an individual or a company that provides MolPort-001-779-720 active pharmaceutical ingredient (API) or MolPort-001-779-720 finished formulations upon request. The MolPort-001-779-720 suppliers may include MolPort-001-779-720 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-001-779-720 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-001-779-720 GMP

MolPort-001-779-720 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-001-779-720 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-001-779-720 GMP manufacturer or MolPort-001-779-720 GMP API supplier for your needs.

MolPort-001-779-720 CoA

A MolPort-001-779-720 CoA (Certificate of Analysis) is a formal document that attests to MolPort-001-779-720's compliance with MolPort-001-779-720 specifications and serves as a tool for batch-level quality control.

MolPort-001-779-720 CoA mostly includes findings from lab analyses of a specific batch. For each MolPort-001-779-720 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-001-779-720 may be tested according to a variety of international standards, such as European Pharmacopoeia (MolPort-001-779-720 EP), MolPort-001-779-720 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MolPort-001-779-720 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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