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Looking for 83763-15-9 / Agn-Pc-0Jl0Lp API manufacturers, exporters & distributors?

Agn-Pc-0Jl0Lp manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Agn-Pc-0Jl0Lp 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 Agn-Pc-0Jl0Lp manufacturer or Agn-Pc-0Jl0Lp supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Agn-Pc-0Jl0Lp manufacturer or Agn-Pc-0Jl0Lp supplier.

PharmaCompass also assists you with knowing the Agn-Pc-0Jl0Lp API Price utilized in the formulation of products. Agn-Pc-0Jl0Lp API Price is not always fixed or binding as the Agn-Pc-0Jl0Lp Price is obtained through a variety of data sources. The Agn-Pc-0Jl0Lp Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Agn-Pc-0Jl0Lp

Synonyms

83763-15-9, Ethyl 4-(2,3-dihydro-2-oxo-1h-benzimidazol-1-yl)-3,6-dihydro-2h-pyridine-1-carboxylate, 87f98555ka, Einecs 280-699-9, Unii-87f98555ka, Dtxsid00232607

Cas Number

83763-15-9

Unique Ingredient Identifier (UNII)

87F98555KA

Agn-Pc-0Jl0Lp Manufacturers

A Agn-Pc-0Jl0Lp manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Agn-Pc-0Jl0Lp, including repackagers and relabelers. The FDA regulates Agn-Pc-0Jl0Lp manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Agn-Pc-0Jl0Lp API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Agn-Pc-0Jl0Lp Suppliers

A Agn-Pc-0Jl0Lp supplier is an individual or a company that provides Agn-Pc-0Jl0Lp active pharmaceutical ingredient (API) or Agn-Pc-0Jl0Lp finished formulations upon request. The Agn-Pc-0Jl0Lp suppliers may include Agn-Pc-0Jl0Lp API manufacturers, exporters, distributors and traders.

click here to find a list of Agn-Pc-0Jl0Lp suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Agn-Pc-0Jl0Lp USDMF

A Agn-Pc-0Jl0Lp DMF (Drug Master File) is a document detailing the whole manufacturing process of Agn-Pc-0Jl0Lp active pharmaceutical ingredient (API) in detail. Different forms of Agn-Pc-0Jl0Lp DMFs exist exist since differing nations have different regulations, such as Agn-Pc-0Jl0Lp USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Agn-Pc-0Jl0Lp DMF submitted to regulatory agencies in the US is known as a USDMF. Agn-Pc-0Jl0Lp USDMF includes data on Agn-Pc-0Jl0Lp's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Agn-Pc-0Jl0Lp USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Agn-Pc-0Jl0Lp suppliers with USDMF on PharmaCompass.

Agn-Pc-0Jl0Lp GMP

Agn-Pc-0Jl0Lp 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 Agn-Pc-0Jl0Lp 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 Agn-Pc-0Jl0Lp GMP manufacturer or Agn-Pc-0Jl0Lp GMP API supplier for your needs.

Agn-Pc-0Jl0Lp CoA

A Agn-Pc-0Jl0Lp CoA (Certificate of Analysis) is a formal document that attests to Agn-Pc-0Jl0Lp's compliance with Agn-Pc-0Jl0Lp specifications and serves as a tool for batch-level quality control.

Agn-Pc-0Jl0Lp CoA mostly includes findings from lab analyses of a specific batch. For each Agn-Pc-0Jl0Lp 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.

Agn-Pc-0Jl0Lp may be tested according to a variety of international standards, such as European Pharmacopoeia (Agn-Pc-0Jl0Lp EP), Agn-Pc-0Jl0Lp JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Agn-Pc-0Jl0Lp 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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