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01 Teva Pharmaceutical Works Private Limited Company (1)
01 Tobramycin "Teva" (1)
01 Israel (1)
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PharmaCompass offers a list of Tobramycin 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 Tobramycin manufacturer or Tobramycin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tobramycin manufacturer or Tobramycin supplier.
PharmaCompass also assists you with knowing the Tobramycin API Price utilized in the formulation of products. Tobramycin API Price is not always fixed or binding as the Tobramycin Price is obtained through a variety of data sources. The Tobramycin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Alveoterol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alveoterol, including repackagers and relabelers. The FDA regulates Alveoterol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alveoterol 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 Alveoterol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Alveoterol supplier is an individual or a company that provides Alveoterol active pharmaceutical ingredient (API) or Alveoterol finished formulations upon request. The Alveoterol suppliers may include Alveoterol API manufacturers, exporters, distributors and traders.
click here to find a list of Alveoterol 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 Alveoterol Drug Master File in Japan (Alveoterol JDMF) empowers Alveoterol 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 Alveoterol JDMF during the approval evaluation for pharmaceutical products. At the time of Alveoterol 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 Alveoterol suppliers with JDMF on PharmaCompass.
