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
A Noscapine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Noscapine, including repackagers and relabelers. The FDA regulates Noscapine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Noscapine 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 Noscapine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Noscapine supplier is an individual or a company that provides Noscapine active pharmaceutical ingredient (API) or Noscapine finished formulations upon request. The Noscapine suppliers may include Noscapine API manufacturers, exporters, distributors and traders.
click here to find a list of Noscapine 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 Noscapine Drug Master File in Japan (Noscapine JDMF) empowers Noscapine 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 Noscapine JDMF during the approval evaluation for pharmaceutical products. At the time of Noscapine 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 Noscapine suppliers with JDMF on PharmaCompass.
We have 3 companies offering Noscapine
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