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DRUG PRODUCT COMPOSITIONS
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 BYDUREON PEN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BYDUREON PEN, including repackagers and relabelers. The FDA regulates BYDUREON PEN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BYDUREON PEN 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 BYDUREON PEN supplier is an individual or a company that provides BYDUREON PEN active pharmaceutical ingredient (API) or BYDUREON PEN finished formulations upon request. The BYDUREON PEN suppliers may include BYDUREON PEN API manufacturers, exporters, distributors and traders.
click here to find a list of BYDUREON PEN suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A BYDUREON PEN DMF (Drug Master File) is a document detailing the whole manufacturing process of BYDUREON PEN active pharmaceutical ingredient (API) in detail. Different forms of BYDUREON PEN DMFs exist exist since differing nations have different regulations, such as BYDUREON PEN USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A BYDUREON PEN DMF submitted to regulatory agencies in the US is known as a USDMF. BYDUREON PEN USDMF includes data on BYDUREON PEN's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The BYDUREON PEN USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of BYDUREON PEN suppliers with USDMF on PharmaCompass.
BYDUREON PEN 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 BYDUREON PEN 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 BYDUREON PEN GMP manufacturer or BYDUREON PEN GMP API supplier for your needs.
A BYDUREON PEN CoA (Certificate of Analysis) is a formal document that attests to BYDUREON PEN's compliance with BYDUREON PEN specifications and serves as a tool for batch-level quality control.
BYDUREON PEN CoA mostly includes findings from lab analyses of a specific batch. For each BYDUREON PEN 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.
BYDUREON PEN may be tested according to a variety of international standards, such as European Pharmacopoeia (BYDUREON PEN EP), BYDUREON PEN JP (Japanese Pharmacopeia) and the US Pharmacopoeia (BYDUREON PEN USP).
