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01 BASF Corporation (1)
02 SI Group, Inc. (1)
03 Sogo Yakuko Co., Ltd. (1)
04 Solara Active Pharma Sciences Limited (1)
01 Ibuprofen (2)
02 Ibuprofen Ibuprofen (1)
03 Ibuprofen pico Nord (1)
01 Germany (1)
02 India (1)
03 Japan (1)
04 U.S.A (1)
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PharmaCompass offers a list of Ibuprofen 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 Ibuprofen manufacturer or Ibuprofen supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ibuprofen manufacturer or Ibuprofen supplier.
PharmaCompass also assists you with knowing the Ibuprofen API Price utilized in the formulation of products. Ibuprofen API Price is not always fixed or binding as the Ibuprofen Price is obtained through a variety of data sources. The Ibuprofen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AM20060782 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AM20060782, including repackagers and relabelers. The FDA regulates AM20060782 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AM20060782 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 AM20060782 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AM20060782 supplier is an individual or a company that provides AM20060782 active pharmaceutical ingredient (API) or AM20060782 finished formulations upon request. The AM20060782 suppliers may include AM20060782 API manufacturers, exporters, distributors and traders.
click here to find a list of AM20060782 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 AM20060782 Drug Master File in Japan (AM20060782 JDMF) empowers AM20060782 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 AM20060782 JDMF during the approval evaluation for pharmaceutical products. At the time of AM20060782 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 AM20060782 suppliers with JDMF on PharmaCompass.
We have 4 companies offering AM20060782
Get in contact with the supplier of your choice:
