01 1Alives Life Sciences Limited
02 1Chongqing Huapont Shengchem Pharm. Co. , Ltd.
03 1Curia Spain S. A. U.
04 1F. I. S. Fabrica Italiana Sintetici S. p. A.
05 1KOLON LIFE SCIENCE, INC.
06 1Kyowa Pharma Chemical Co., Ltd.
07 1MSN Laboratories Private Limited.
08 2Sumitomo Chemical Co., Ltd.
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PharmaCompass offers a list of Olopatadine 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 Olopatadine Hydrochloride manufacturer or Olopatadine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Olopatadine Hydrochloride manufacturer or Olopatadine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Olopatadine Hydrochloride API Price utilized in the formulation of products. Olopatadine Hydrochloride API Price is not always fixed or binding as the Olopatadine Hydrochloride Price is obtained through a variety of data sources. The Olopatadine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PAZEO manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PAZEO, including repackagers and relabelers. The FDA regulates PAZEO manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PAZEO 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 PAZEO manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PAZEO supplier is an individual or a company that provides PAZEO active pharmaceutical ingredient (API) or PAZEO finished formulations upon request. The PAZEO suppliers may include PAZEO API manufacturers, exporters, distributors and traders.
click here to find a list of PAZEO 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 PAZEO Drug Master File in Japan (PAZEO JDMF) empowers PAZEO 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 PAZEO JDMF during the approval evaluation for pharmaceutical products. At the time of PAZEO 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 PAZEO suppliers with JDMF on PharmaCompass.
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