01 1HAS Healthcare Advanced Synthesis SA
02 1Patheon Austria GmbH & Co KG
01 2Pyridostigmine bromide
01 1Switzerland
02 1U.S.A
Registration Number : 221MF10103
Registrant's Address : Via Industria, 24 6710 Biasca Switzerland
Initial Date of Registration : 2009-05-27
Latest Date of Registration : 2009-05-27
Registration Number : 227MF10212
Registrant's Address : St. -Peter-Strasse 25, 4020 Linz / Austria
Initial Date of Registration : 2015-08-18
Latest Date of Registration : 2015-08-18
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PharmaCompass offers a list of Pyridostigmine 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 Pyridostigmine manufacturer or Pyridostigmine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pyridostigmine manufacturer or Pyridostigmine supplier.
PharmaCompass also assists you with knowing the Pyridostigmine API Price utilized in the formulation of products. Pyridostigmine API Price is not always fixed or binding as the Pyridostigmine Price is obtained through a variety of data sources. The Pyridostigmine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lefaxin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lefaxin, including repackagers and relabelers. The FDA regulates Lefaxin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lefaxin 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 Lefaxin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lefaxin supplier is an individual or a company that provides Lefaxin active pharmaceutical ingredient (API) or Lefaxin finished formulations upon request. The Lefaxin suppliers may include Lefaxin API manufacturers, exporters, distributors and traders.
click here to find a list of Lefaxin 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 Lefaxin Drug Master File in Japan (Lefaxin JDMF) empowers Lefaxin 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 Lefaxin JDMF during the approval evaluation for pharmaceutical products. At the time of Lefaxin 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 Lefaxin suppliers with JDMF on PharmaCompass.
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