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, Price,and more, enabling you to easily find the right Salbutamol Sulphate manufacturer or Salbutamol Sulphate supplier for your needs.
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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 [USP IMPURITY] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALBUTEROL SULFATE [USP IMPURITY], including repackagers and relabelers. The FDA regulates ALBUTEROL SULFATE [USP IMPURITY] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALBUTEROL SULFATE [USP IMPURITY] 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 [USP IMPURITY] supplier is an individual or a company that provides ALBUTEROL SULFATE [USP IMPURITY] active pharmaceutical ingredient (API) or ALBUTEROL SULFATE [USP IMPURITY] finished formulations upon request. The ALBUTEROL SULFATE [USP IMPURITY] suppliers may include ALBUTEROL SULFATE [USP IMPURITY] API manufacturers, exporters, distributors and traders.
click here to find a list of ALBUTEROL SULFATE [USP IMPURITY] 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 [USP IMPURITY] Drug Master File in Japan (ALBUTEROL SULFATE [USP IMPURITY] JDMF) empowers ALBUTEROL SULFATE [USP IMPURITY] 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 [USP IMPURITY] JDMF during the approval evaluation for pharmaceutical products. At the time of ALBUTEROL SULFATE [USP IMPURITY] 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 [USP IMPURITY] suppliers with JDMF on PharmaCompass.
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