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
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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