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PharmaCompass offers a list of Paracetamol 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 Paracetamol manufacturer or Paracetamol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Paracetamol manufacturer or Paracetamol supplier.
PharmaCompass also assists you with knowing the Paracetamol API Price utilized in the formulation of products. Paracetamol API Price is not always fixed or binding as the Paracetamol Price is obtained through a variety of data sources. The Paracetamol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Acetaminophen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acetaminophen, including repackagers and relabelers. The FDA regulates Acetaminophen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acetaminophen 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 Acetaminophen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acetaminophen supplier is an individual or a company that provides Acetaminophen active pharmaceutical ingredient (API) or Acetaminophen finished formulations upon request. The Acetaminophen suppliers may include Acetaminophen API manufacturers, exporters, distributors and traders.
click here to find a list of Acetaminophen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Acetaminophen Drug Master File in Japan (Acetaminophen JDMF) empowers Acetaminophen 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 Acetaminophen JDMF during the approval evaluation for pharmaceutical products. At the time of Acetaminophen 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 Acetaminophen suppliers with JDMF on PharmaCompass.
We have 10 companies offering Acetaminophen
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