01 1Esteve Quimica, S. A.
02 1Guilin Hwasun Pharmaceutical Co. , Ltd.
03 1Pharmacostech CO. ,LTD
04 1Quimica Syntetica S. A.
05 1SHOUGUANG FUKANG PHARMACEUTICAL CO. , LTD.
06 2TAPI Croatia Industries Ltd.
07 1Zhejiang Huayi Pharmaceutical Co. , Ltd.
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PharmaCompass offers a list of Omeprazole 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 Omeprazole manufacturer or Omeprazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Omeprazole manufacturer or Omeprazole supplier.
PharmaCompass also assists you with knowing the Omeprazole API Price utilized in the formulation of products. Omeprazole API Price is not always fixed or binding as the Omeprazole Price is obtained through a variety of data sources. The Omeprazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Antra manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Antra, including repackagers and relabelers. The FDA regulates Antra manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Antra 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 Antra manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Antra supplier is an individual or a company that provides Antra active pharmaceutical ingredient (API) or Antra finished formulations upon request. The Antra suppliers may include Antra API manufacturers, exporters, distributors and traders.
click here to find a list of Antra 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 Antra Drug Master File in Japan (Antra JDMF) empowers Antra 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 Antra JDMF during the approval evaluation for pharmaceutical products. At the time of Antra 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 Antra suppliers with JDMF on PharmaCompass.
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