01 1PEPTIDO GmbH
02 1Sandoz GmbH
01 1Levothyroxine sodium
02 1Levothyroxine sodium hydrate
01 1Germany
02 1Switzerland
Registration Number : 221MF10168
Registrant's Address : Am Kraftwerk 6, D-66450 Bexbach, Germany
Initial Date of Registration : 2009-07-30
Latest Date of Registration : 2009-07-30
Registration Number : 217MF10456
Registrant's Address : Biochemiesstrasse 10, 6250 Kundl, Austria
Initial Date of Registration : 2005-08-24
Latest Date of Registration : 2017-12-06
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PharmaCompass offers a list of Levothyroxine Sodium 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 Levothyroxine Sodium manufacturer or Levothyroxine Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levothyroxine Sodium manufacturer or Levothyroxine Sodium supplier.
PharmaCompass also assists you with knowing the Levothyroxine Sodium API Price utilized in the formulation of products. Levothyroxine Sodium API Price is not always fixed or binding as the Levothyroxine Sodium Price is obtained through a variety of data sources. The Levothyroxine Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Leo, Tiroxina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Leo, Tiroxina, including repackagers and relabelers. The FDA regulates Leo, Tiroxina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Leo, Tiroxina API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Leo, Tiroxina supplier is an individual or a company that provides Leo, Tiroxina active pharmaceutical ingredient (API) or Leo, Tiroxina finished formulations upon request. The Leo, Tiroxina suppliers may include Leo, Tiroxina API manufacturers, exporters, distributors and traders.
click here to find a list of Leo, Tiroxina 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 Leo, Tiroxina Drug Master File in Japan (Leo, Tiroxina JDMF) empowers Leo, Tiroxina 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 Leo, Tiroxina JDMF during the approval evaluation for pharmaceutical products. At the time of Leo, Tiroxina JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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