Cosma S.p.A., part of CFM Group with AMSA & Clarochem, provides global pharma & veterinary health with 300+ tons of FDA-approved APIs.

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01 1COSMA S. P. A.
02 1Ipca Laboratories Limited
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01 1Propranolol hydrochloride
02 1Propranolol hydrochloride (production only)
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01 1India
02 1Italy
Cosma S.p.A., part of CFM Group with AMSA & Clarochem, provides global pharma & veterinary health with 300+ tons of FDA-approved APIs.
Propranolol hydrochloride (for manufacturing purposes 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 : 2026-03-03
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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A AY20694 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AY20694, including repackagers and relabelers. The FDA regulates AY20694 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AY20694 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 AY20694 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A AY20694 supplier is an individual or a company that provides AY20694 active pharmaceutical ingredient (API) or AY20694 finished formulations upon request. The AY20694 suppliers may include AY20694 API manufacturers, exporters, distributors and traders.
click here to find a list of AY20694 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 AY20694 Drug Master File in Japan (AY20694 JDMF) empowers AY20694 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 AY20694 JDMF during the approval evaluation for pharmaceutical products. At the time of AY20694 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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