01 1Dipharma Francis S. r. l.
02 1Olon S. p. A.
01 2Cyproheptadine hydrochloride hydrate
01 2Italy
Cyproheptadine hydrochloride hydrate
Registration Number : 220MF10221
Registrant's Address : Via Bissone, 5, 20021-Baranzate, Milano, Italy
Initial Date of Registration : 2008-11-04
Latest Date of Registration : 2022-06-28
Cyproheptadine hydrochloride hydrate
Registration Number : 220MF10143
Registrant's Address : Strada Rivoltana Km 6/7 20053 Rodano Milano Italy
Initial Date of Registration : 2008-06-10
Latest Date of Registration : 2021-09-28
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PharmaCompass also assists you with knowing the Cyproheptadine Hydrochloride API Price utilized in the formulation of products. Cyproheptadine Hydrochloride API Price is not always fixed or binding as the Cyproheptadine Hydrochloride Price is obtained through a variety of data sources. The Cyproheptadine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A anhydraous cyproheptadine hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of anhydraous cyproheptadine hydrochloride, including repackagers and relabelers. The FDA regulates anhydraous cyproheptadine hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. anhydraous cyproheptadine hydrochloride 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 anhydraous cyproheptadine hydrochloride supplier is an individual or a company that provides anhydraous cyproheptadine hydrochloride active pharmaceutical ingredient (API) or anhydraous cyproheptadine hydrochloride finished formulations upon request. The anhydraous cyproheptadine hydrochloride suppliers may include anhydraous cyproheptadine hydrochloride API manufacturers, exporters, distributors and traders.
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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 anhydraous cyproheptadine hydrochloride Drug Master File in Japan (anhydraous cyproheptadine hydrochloride JDMF) empowers anhydraous cyproheptadine hydrochloride 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 anhydraous cyproheptadine hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of anhydraous cyproheptadine hydrochloride 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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