01 1Boehringer Ingelheim Pharma GmbH & Co. K.G.
01 1Ipratropium bromide hydrate
01 1Germany
Registration Number : 220MF10081
Registrant's Address : Binger Strasse 173,55216 Ingelheim am Rhein
Initial Date of Registration : 2008-03-14
Latest Date of Registration : 2023-11-08
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PharmaCompass offers a list of Ipratropium Bromide 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 Ipratropium Bromide manufacturer or Ipratropium Bromide supplier for your needs.
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PharmaCompass also assists you with knowing the Ipratropium Bromide API Price utilized in the formulation of products. Ipratropium Bromide API Price is not always fixed or binding as the Ipratropium Bromide Price is obtained through a variety of data sources. The Ipratropium Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Itrop manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Itrop, including repackagers and relabelers. The FDA regulates Itrop manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Itrop 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 Itrop manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Itrop supplier is an individual or a company that provides Itrop active pharmaceutical ingredient (API) or Itrop finished formulations upon request. The Itrop suppliers may include Itrop API manufacturers, exporters, distributors and traders.
click here to find a list of Itrop 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 Itrop Drug Master File in Japan (Itrop JDMF) empowers Itrop 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 Itrop JDMF during the approval evaluation for pharmaceutical products. At the time of Itrop JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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