01 1Cambrex Profarmaco Milano S. r. l.
01 1Salbutamol sulphate
01 1U.S.A
Registration Number : 219MF10285
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2007-09-10
Latest Date of Registration : 2025-03-26
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PharmaCompass offers a list of Salbutamol Sulphate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Salbutamol Sulphate manufacturer or Salbutamol Sulphate supplier for your needs.
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A Salbutamol Diskus manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Salbutamol Diskus, including repackagers and relabelers. The FDA regulates Salbutamol Diskus manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Salbutamol Diskus 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 Salbutamol Diskus manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Salbutamol Diskus supplier is an individual or a company that provides Salbutamol Diskus active pharmaceutical ingredient (API) or Salbutamol Diskus finished formulations upon request. The Salbutamol Diskus suppliers may include Salbutamol Diskus API manufacturers, exporters, distributors and traders.
click here to find a list of Salbutamol Diskus suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Salbutamol Diskus Drug Master File in Japan (Salbutamol Diskus JDMF) empowers Salbutamol Diskus 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 Salbutamol Diskus JDMF during the approval evaluation for pharmaceutical products. At the time of Salbutamol Diskus 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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