01 1SpecGx LLC
01 1Methadone hydrochloride
01 1Ireland
Registration Number : 223MF10179
Registrant's Address : 385 Marshall Ave, Webster Groves, Missouri 63119, United States
Initial Date of Registration : 2011-12-27
Latest Date of Registration : 2012-09-14
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PharmaCompass offers a list of Methadone 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 Methadone Hydrochloride manufacturer or Methadone Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methadone Hydrochloride manufacturer or Methadone Hydrochloride supplier.
PharmaCompass also assists you with knowing the Methadone Hydrochloride API Price utilized in the formulation of products. Methadone Hydrochloride API Price is not always fixed or binding as the Methadone Hydrochloride Price is obtained through a variety of data sources. The Methadone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mecodin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mecodin, including repackagers and relabelers. The FDA regulates Mecodin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mecodin 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 Mecodin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mecodin supplier is an individual or a company that provides Mecodin active pharmaceutical ingredient (API) or Mecodin finished formulations upon request. The Mecodin suppliers may include Mecodin API manufacturers, exporters, distributors and traders.
click here to find a list of Mecodin 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 Mecodin Drug Master File in Japan (Mecodin JDMF) empowers Mecodin 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 Mecodin JDMF during the approval evaluation for pharmaceutical products. At the time of Mecodin 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 Mecodin suppliers with JDMF on PharmaCompass.
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