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DOSAGE - SUSPENSION, EXTENDED RELEASE;SUBCUTA...DOSAGE - SUSPENSION, EXTENDED RELEASE;SUBCUTANEOUS - 2MG/0.85ML (2MG/0.85ML)
USFDA APPLICATION NUMBER - 209210
DOSAGE - INJECTABLE;SUBCUTANEOUS - 300MCG/1.2...DOSAGE - INJECTABLE;SUBCUTANEOUS - 300MCG/1.2ML (250MCG/ML)
USFDA APPLICATION NUMBER - 21773
DOSAGE - INJECTABLE;SUBCUTANEOUS - 600MCG/2.4...DOSAGE - INJECTABLE;SUBCUTANEOUS - 600MCG/2.4ML (250MCG/ML)
USFDA APPLICATION NUMBER - 21773
DOSAGE - FOR SUSPENSION, EXTENDED RELEASE;SUB...DOSAGE - FOR SUSPENSION, EXTENDED RELEASE;SUBCUTANEOUS - 2MG/VIAL
USFDA APPLICATION NUMBER - 22200
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PharmaCompass offers a list of Exenatide Synthetic 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 Exenatide Synthetic manufacturer or Exenatide Synthetic supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Exenatide Synthetic manufacturer or Exenatide Synthetic supplier.
PharmaCompass also assists you with knowing the Exenatide Synthetic API Price utilized in the formulation of products. Exenatide Synthetic API Price is not always fixed or binding as the Exenatide Synthetic Price is obtained through a variety of data sources. The Exenatide Synthetic Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ITCA 650 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ITCA 650, including repackagers and relabelers. The FDA regulates ITCA 650 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ITCA 650 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A ITCA 650 supplier is an individual or a company that provides ITCA 650 active pharmaceutical ingredient (API) or ITCA 650 finished formulations upon request. The ITCA 650 suppliers may include ITCA 650 API manufacturers, exporters, distributors and traders.
click here to find a list of ITCA 650 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ITCA 650 DMF (Drug Master File) is a document detailing the whole manufacturing process of ITCA 650 active pharmaceutical ingredient (API) in detail. Different forms of ITCA 650 DMFs exist exist since differing nations have different regulations, such as ITCA 650 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A ITCA 650 DMF submitted to regulatory agencies in the US is known as a USDMF. ITCA 650 USDMF includes data on ITCA 650's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The ITCA 650 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of ITCA 650 suppliers with USDMF on PharmaCompass.
ITCA 650 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 ITCA 650 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 ITCA 650 GMP manufacturer or ITCA 650 GMP API supplier for your needs.
A ITCA 650 CoA (Certificate of Analysis) is a formal document that attests to ITCA 650's compliance with ITCA 650 specifications and serves as a tool for batch-level quality control.
ITCA 650 CoA mostly includes findings from lab analyses of a specific batch. For each ITCA 650 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.
ITCA 650 may be tested according to a variety of international standards, such as European Pharmacopoeia (ITCA 650 EP), ITCA 650 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (ITCA 650 USP).
