Temad- We think of world-class quality.
01 1TEMAD CO ACTIVE PHARMACEUTICAL INGREDIENTS
02 1Shiratori Pharmaceutical Co., Ltd.
03 1Takeda Pharmaceutical Company Limited
01 1Japanese Pharmacopoeia noscapine
02 1Noscapine
03 1Only the Japanese Pharmacopoeia noscapine production
01 1Iran
02 2Japan
Temad- We think of world-class quality.
Japanese Pharmacopoeia Noscapine
Registration Number : 219MF10150
Registrant's Address : 28th Km of Karaj Makhsous Road, Tehran, Iran
Initial Date of Registration : 2007-04-27
Latest Date of Registration : 2007-04-27
Japanese Pharmacopoeia Noscapine For manufacturing only
Registration Number : 217MF10315
Registrant's Address : 6-11-24 Tsudanuma, Narashino City, Chiba Prefecture
Initial Date of Registration : 2005-07-14
Latest Date of Registration : 2008-11-04
Registration Number : 218MF10578
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Doshomachi 4-1-1
Initial Date of Registration : 2006-06-22
Latest Date of Registration : 2008-06-30
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PharmaCompass offers a list of Noscapine 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 Noscapine manufacturer or Noscapine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Noscapine manufacturer or Noscapine supplier.
PharmaCompass also assists you with knowing the Noscapine API Price utilized in the formulation of products. Noscapine API Price is not always fixed or binding as the Noscapine Price is obtained through a variety of data sources. The Noscapine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tuscalman manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tuscalman, including repackagers and relabelers. The FDA regulates Tuscalman manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tuscalman 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 Tuscalman manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tuscalman supplier is an individual or a company that provides Tuscalman active pharmaceutical ingredient (API) or Tuscalman finished formulations upon request. The Tuscalman suppliers may include Tuscalman API manufacturers, exporters, distributors and traders.
click here to find a list of Tuscalman 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 Tuscalman Drug Master File in Japan (Tuscalman JDMF) empowers Tuscalman 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 Tuscalman JDMF during the approval evaluation for pharmaceutical products. At the time of Tuscalman 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 Tuscalman suppliers with JDMF on PharmaCompass.
We have 3 companies offering Tuscalman
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