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PharmaCompass offers a list of Latanoprost 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 Latanoprost manufacturer or Latanoprost supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Latanoprost manufacturer or Latanoprost supplier.
PharmaCompass also assists you with knowing the Latanoprost API Price utilized in the formulation of products. Latanoprost API Price is not always fixed or binding as the Latanoprost Price is obtained through a variety of data sources. The Latanoprost Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Latanoprost manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Latanoprost, including repackagers and relabelers. The FDA regulates Latanoprost manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Latanoprost 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 Latanoprost manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Latanoprost supplier is an individual or a company that provides Latanoprost active pharmaceutical ingredient (API) or Latanoprost finished formulations upon request. The Latanoprost suppliers may include Latanoprost API manufacturers, exporters, distributors and traders.
click here to find a list of Latanoprost 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 Latanoprost Drug Master File in Japan (Latanoprost JDMF) empowers Latanoprost 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 Latanoprost JDMF during the approval evaluation for pharmaceutical products. At the time of Latanoprost 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 Latanoprost suppliers with JDMF on PharmaCompass.
We have 7 companies offering Latanoprost
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