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 also assists you with knowing the Salbutamol Sulphate API Price utilized in the formulation of products. Salbutamol Sulphate API Price is not always fixed or binding as the Salbutamol Sulphate Price is obtained through a variety of data sources. The Salbutamol Sulphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE, including repackagers and relabelers. The FDA regulates ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE supplier is an individual or a company that provides ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE active pharmaceutical ingredient (API) or ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE finished formulations upon request. The ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE suppliers may include ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE API manufacturers, exporters, distributors and traders.
click here to find a list of ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE 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 ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE Drug Master File in Japan (ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE JDMF) empowers ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE 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 ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE JDMF during the approval evaluation for pharmaceutical products. At the time of ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE 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 ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE suppliers with JDMF on PharmaCompass.
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