Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
01 1Chunghwa Chemical Synthesis & Biotech Co. , Ltd.
02 1Zhejiang Haizhou Pharmaceutical Co. , Ltd.
01 1External regulations Methocarbamol (for manufacturing only)
02 1Methocarbamol
01 1China
02 1Taiwan
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Methocarbamol (for manufacturing only)
Registration Number : 218MF10061
Registrant's Address : No. 1, Tung-Hsing St. , Shu-Lin, New Taipei City 23850, Taiwan
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2015-01-23
Registration Number : 306MF10019
Registrant's Address : Yunxi Road 147#, Jiaojiang, Taizhou, Zhejiang, China
Initial Date of Registration : 2024-01-30
Latest Date of Registration : 2024-01-30
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PharmaCompass offers a list of Methocarbamol 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 Methocarbamol manufacturer or Methocarbamol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methocarbamol manufacturer or Methocarbamol supplier.
PharmaCompass also assists you with knowing the Methocarbamol API Price utilized in the formulation of products. Methocarbamol API Price is not always fixed or binding as the Methocarbamol Price is obtained through a variety of data sources. The Methocarbamol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Methocarbamol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methocarbamol, including repackagers and relabelers. The FDA regulates Methocarbamol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methocarbamol 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 Methocarbamol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methocarbamol supplier is an individual or a company that provides Methocarbamol active pharmaceutical ingredient (API) or Methocarbamol finished formulations upon request. The Methocarbamol suppliers may include Methocarbamol API manufacturers, exporters, distributors and traders.
click here to find a list of Methocarbamol 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 Methocarbamol Drug Master File in Japan (Methocarbamol JDMF) empowers Methocarbamol 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 Methocarbamol JDMF during the approval evaluation for pharmaceutical products. At the time of Methocarbamol 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 Methocarbamol suppliers with JDMF on PharmaCompass.
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