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
A Doxycycline Hyclate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Doxycycline Hyclate, including repackagers and relabelers. The FDA regulates Doxycycline Hyclate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Doxycycline Hyclate 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 Doxycycline Hyclate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Doxycycline Hyclate supplier is an individual or a company that provides Doxycycline Hyclate active pharmaceutical ingredient (API) or Doxycycline Hyclate finished formulations upon request. The Doxycycline Hyclate suppliers may include Doxycycline Hyclate API manufacturers, exporters, distributors and traders.
click here to find a list of Doxycycline Hyclate 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 Doxycycline Hyclate Drug Master File in Japan (Doxycycline Hyclate JDMF) empowers Doxycycline Hyclate 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 Doxycycline Hyclate JDMF during the approval evaluation for pharmaceutical products. At the time of Doxycycline Hyclate 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 Doxycycline Hyclate suppliers with JDMF on PharmaCompass.
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