Cosma S.p.A.: FDA-approved API manufacturing with 300+ tons capacity, serving pharma and animal health industries worldwide.
01 1COSMA S. P. A.
02 1Ipca Laboratories Limited
01 1Propranolol hydrochloride
02 1Propranolol hydrochloride (production only)
01 1India
02 1Italy
Cosma S.p.A.: FDA-approved API manufacturing with 300+ tons capacity, serving pharma and animal health industries worldwide.
Propranolol hydrochloride (for manufacturing only)
Registration Number : 221MF10278
Registrant's Address : Via Colleoni 15/17, 24040 Ciserano (BG)・Italy
Initial Date of Registration : 2009-12-18
Latest Date of Registration : 2016-03-11
Registration Number : 218MF10174
Registrant's Address : 48, Kandivli Industrial Estate, Kandivli (W), Mumbai 400 067, India
Initial Date of Registration : 2006-02-08
Latest Date of Registration : 2006-10-20
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PharmaCompass offers a list of Propranolol Hydrochloride 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 Propranolol Hydrochloride manufacturer or Propranolol Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Propranolol Hydrochloride API Price utilized in the formulation of products. Propranolol Hydrochloride API Price is not always fixed or binding as the Propranolol Hydrochloride Price is obtained through a variety of data sources. The Propranolol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A KDM-1102 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KDM-1102, including repackagers and relabelers. The FDA regulates KDM-1102 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KDM-1102 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 KDM-1102 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A KDM-1102 supplier is an individual or a company that provides KDM-1102 active pharmaceutical ingredient (API) or KDM-1102 finished formulations upon request. The KDM-1102 suppliers may include KDM-1102 API manufacturers, exporters, distributors and traders.
click here to find a list of KDM-1102 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 KDM-1102 Drug Master File in Japan (KDM-1102 JDMF) empowers KDM-1102 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 KDM-1102 JDMF during the approval evaluation for pharmaceutical products. At the time of KDM-1102 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 KDM-1102 suppliers with JDMF on PharmaCompass.
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