01 2Loba biotech GmbH
01 2Naphazoline Nitrate (for manufacturing only)
01 2Austria
Naphazoline nitrate (for manufacturing only)
Registration Number : 231MF10042
Registrant's Address : Fehrgasse 7 A-2401 Fischamend, Austria
Initial Date of Registration : 2019-02-13
Latest Date of Registration : 2019-02-13
Naphazoline nitrate (for manufacturing only)
Registration Number : 221MF10084
Registrant's Address : Fehrgasse 7 A-2401 Fischamend, Austria
Initial Date of Registration : 2009-04-22
Latest Date of Registration : 2018-09-14
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PharmaCompass offers a list of Naphazoline Nitrate 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 Naphazoline Nitrate manufacturer or Naphazoline Nitrate supplier for your needs.
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A Febena Brand of Naphazoline Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Febena Brand of Naphazoline Hydrochloride, including repackagers and relabelers. The FDA regulates Febena Brand of Naphazoline Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Febena Brand of Naphazoline 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 Febena Brand of Naphazoline Hydrochloride supplier is an individual or a company that provides Febena Brand of Naphazoline Hydrochloride active pharmaceutical ingredient (API) or Febena Brand of Naphazoline Hydrochloride finished formulations upon request. The Febena Brand of Naphazoline Hydrochloride suppliers may include Febena Brand of Naphazoline Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Febena Brand of Naphazoline Hydrochloride 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 Febena Brand of Naphazoline Hydrochloride Drug Master File in Japan (Febena Brand of Naphazoline Hydrochloride JDMF) empowers Febena Brand of Naphazoline 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 Febena Brand of Naphazoline Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Febena Brand of Naphazoline 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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