01 1Hovione PharmaScience Limited
01 1Doxycycline hyclate
01 1Portugal
Registration Number : 224MF10204
Registrant's Address : Estrada Coronel Nicolau de Mesquita Taipa, Macau S. A. R. China
Initial Date of Registration : 2012-10-09
Latest Date of Registration : 2024-05-15
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PharmaCompass offers a list of Doxycycline Hyclate 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 Doxycycline Hyclate manufacturer or Doxycycline Hyclate supplier for your needs.
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PharmaCompass also assists you with knowing the Doxycycline Hyclate API Price utilized in the formulation of products. Doxycycline Hyclate API Price is not always fixed or binding as the Doxycycline Hyclate Price is obtained through a variety of data sources. The Doxycycline Hyclate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DOXY 200 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DOXY 200, including repackagers and relabelers. The FDA regulates DOXY 200 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DOXY 200 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 DOXY 200 supplier is an individual or a company that provides DOXY 200 active pharmaceutical ingredient (API) or DOXY 200 finished formulations upon request. The DOXY 200 suppliers may include DOXY 200 API manufacturers, exporters, distributors and traders.
click here to find a list of DOXY 200 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 DOXY 200 Drug Master File in Japan (DOXY 200 JDMF) empowers DOXY 200 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 DOXY 200 JDMF during the approval evaluation for pharmaceutical products. At the time of DOXY 200 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 DOXY 200 suppliers with JDMF on PharmaCompass.
