Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
01 1CENTRIENT PHARMACEUTICALS INDIA PRIVATE LIMITED
02 1DAEWOONG BIO INC.
01 1Cloxacillin sodium hydrate
02 1[Japanese Pharmacopoeia] cloxacillin sodium
01 1Netherlands
02 1South Korea
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Registration Number : 227MF10133
Registrant's Address : Bhai Mohan Singh Nagar, Toansa, District SBS Nagar (Nawanshahr), Punjab-144 533, Indi...
Initial Date of Registration : 2015-04-30
Latest Date of Registration : 2015-04-30
[Japanese Pharmacopoeia] Cloxacillin Sodium
Registration Number : 218MF11024
Registrant's Address : 12 BONGEUNSA-RO, 114-GIL, GANGNAM-GU, SEOUL, 135-715 KOREA
Initial Date of Registration : 2006-12-28
Latest Date of Registration : 2006-12-28
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PharmaCompass also assists you with knowing the Cloxacillin Sodium API Price utilized in the formulation of products. Cloxacillin Sodium API Price is not always fixed or binding as the Cloxacillin Sodium Price is obtained through a variety of data sources. The Cloxacillin Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cloxacillin, Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cloxacillin, Sodium, including repackagers and relabelers. The FDA regulates Cloxacillin, Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cloxacillin, Sodium 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 Cloxacillin, Sodium supplier is an individual or a company that provides Cloxacillin, Sodium active pharmaceutical ingredient (API) or Cloxacillin, Sodium finished formulations upon request. The Cloxacillin, Sodium suppliers may include Cloxacillin, Sodium 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 Cloxacillin, Sodium Drug Master File in Japan (Cloxacillin, Sodium JDMF) empowers Cloxacillin, Sodium 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 Cloxacillin, Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Cloxacillin, Sodium 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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