01 1Active Pharma Co., Ltd.
02 1Assia Chemical Industries Ltd.
03 1Daito Co., Ltd.
04 1JUBILANT BIOSYS LIMITED.
05 1Osaka Synthetic Organic Chemistry Laboratory Co., Ltd.
06 2Shijiazhuang Lonzeal Pharmaceuticals Co. , Ltd.
07 1Sumitomo Chemical Co., Ltd.
08 1Zydus Lifesciences Limited
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PharmaCompass offers a list of Paroxetine Hydrochloride 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 Paroxetine Hydrochloride manufacturer or Paroxetine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Paroxetine Hydrochloride manufacturer or Paroxetine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Paroxetine Hydrochloride API Price utilized in the formulation of products. Paroxetine Hydrochloride API Price is not always fixed or binding as the Paroxetine Hydrochloride Price is obtained through a variety of data sources. The Paroxetine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxetine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxetine, including repackagers and relabelers. The FDA regulates Oxetine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxetine 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 Oxetine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxetine supplier is an individual or a company that provides Oxetine active pharmaceutical ingredient (API) or Oxetine finished formulations upon request. The Oxetine suppliers may include Oxetine API manufacturers, exporters, distributors and traders.
click here to find a list of Oxetine 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 Oxetine Drug Master File in Japan (Oxetine JDMF) empowers Oxetine 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 Oxetine JDMF during the approval evaluation for pharmaceutical products. At the time of Oxetine 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 Oxetine suppliers with JDMF on PharmaCompass.
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