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PharmaCompass offers a list of Tacrolimus 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 Tacrolimus manufacturer or Tacrolimus supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tacrolimus manufacturer or Tacrolimus supplier.
PharmaCompass also assists you with knowing the Tacrolimus API Price utilized in the formulation of products. Tacrolimus API Price is not always fixed or binding as the Tacrolimus Price is obtained through a variety of data sources. The Tacrolimus Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tacrolimus Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tacrolimus Monohydrate, including repackagers and relabelers. The FDA regulates Tacrolimus Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tacrolimus Monohydrate 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 Tacrolimus Monohydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tacrolimus Monohydrate supplier is an individual or a company that provides Tacrolimus Monohydrate active pharmaceutical ingredient (API) or Tacrolimus Monohydrate finished formulations upon request. The Tacrolimus Monohydrate suppliers may include Tacrolimus Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Tacrolimus Monohydrate 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 Tacrolimus Monohydrate Drug Master File in Japan (Tacrolimus Monohydrate JDMF) empowers Tacrolimus Monohydrate 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 Tacrolimus Monohydrate JDMF during the approval evaluation for pharmaceutical products. At the time of Tacrolimus Monohydrate 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 Tacrolimus Monohydrate suppliers with JDMF on PharmaCompass.
We have 6 companies offering Tacrolimus Monohydrate
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