01 2Sandoz GmbH
01 1Benzylpenicillin benzathine (1% Lecithin, 0.2% Tween)
02 1Benzylpenicillin benzatin, 1% lecithin (sterile)
01 2Switzerland
Benzylpenicillin benzathine, 1% lecithin (sterile)
Registration Number : 231MF10072
Registrant's Address : Biochemiesstrasse 10, 6250 Kundl, Austria
Initial Date of Registration : 2019-03-12
Latest Date of Registration : 2024-02-21
Benzylpenicillin Benzathine (1% lecithin, 0.2% Tween)
Registration Number : 229MF10169
Registrant's Address : Biochemiesstrasse 10,6250 Kundl, Austria
Initial Date of Registration : 2017-08-28
Latest Date of Registration : 2019-10-25
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PharmaCompass offers a list of Penicillin G Potassium 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 Penicillin G Potassium manufacturer or Penicillin G Potassium supplier for your needs.
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A Penicillin G Potassium in Plastic Container manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Penicillin G Potassium in Plastic Container, including repackagers and relabelers. The FDA regulates Penicillin G Potassium in Plastic Container manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Penicillin G Potassium in Plastic Container 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 Penicillin G Potassium in Plastic Container supplier is an individual or a company that provides Penicillin G Potassium in Plastic Container active pharmaceutical ingredient (API) or Penicillin G Potassium in Plastic Container finished formulations upon request. The Penicillin G Potassium in Plastic Container suppliers may include Penicillin G Potassium in Plastic Container 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 Penicillin G Potassium in Plastic Container Drug Master File in Japan (Penicillin G Potassium in Plastic Container JDMF) empowers Penicillin G Potassium in Plastic Container 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 Penicillin G Potassium in Plastic Container JDMF during the approval evaluation for pharmaceutical products. At the time of Penicillin G Potassium in Plastic Container 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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