Vital Laboratories – Trusted Global Manufacturer of Quinine and Antimalarial APIs Since 1998
01 1Vital Laboratories Pvt. Ltd.
02 2Active Pharma Co., Ltd.
03 2China Chemical Co., Ltd.
04 1RPG Life Sciences Limited
01 1Japanese Pharmacopoeia Drug nicorandil "(production only)."
02 4Nicorandil
03 1Nicorandil S
01 2India
02 4Japan
Vital Laboratories – Trusted Global Manufacturer of Quinine and Antimalarial APIs Since 1998
Registration Number : 226MF10093
Registrant's Address : 2nd Floor, Plot No. 48, Service Road, Western Express Highway, Vile Parle (East), Mum...
Initial Date of Registration : 2014-05-14
Latest Date of Registration : 2014-05-14
Japanese Pharmacopoeia Drug Nicorandil (For manufacturing purposes only)
Registration Number : 217MF10799
Registrant's Address : 1-6 Tenno Shioyacho, Kure City, Hiroshima Prefecture
Initial Date of Registration : 2005-11-01
Latest Date of Registration : 2006-04-07
Registration Number : 219MF10019
Registrant's Address : 1-6 Tenno Shioyacho, Kure City, Hiroshima Prefecture
Initial Date of Registration : 2007-01-18
Latest Date of Registration : 2007-01-18
Registration Number : 305MF10030
Registrant's Address : RPG House, 463, Dr. Annie Besant Road, Worli, Mumbai 400030, India.
Initial Date of Registration : 2023-03-01
Latest Date of Registration : 2023-03-01
Registration Number : 218MF10660
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2006-07-24
Latest Date of Registration : 2013-11-20
Registration Number : 218MF10355
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2006-03-17
Latest Date of Registration : 2013-11-20
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PharmaCompass offers a list of Nicorandil 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 Nicorandil manufacturer or Nicorandil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nicorandil manufacturer or Nicorandil supplier.
PharmaCompass also assists you with knowing the Nicorandil API Price utilized in the formulation of products. Nicorandil API Price is not always fixed or binding as the Nicorandil Price is obtained through a variety of data sources. The Nicorandil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A N0837 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N0837, including repackagers and relabelers. The FDA regulates N0837 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N0837 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 N0837 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A N0837 supplier is an individual or a company that provides N0837 active pharmaceutical ingredient (API) or N0837 finished formulations upon request. The N0837 suppliers may include N0837 API manufacturers, exporters, distributors and traders.
click here to find a list of N0837 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 N0837 Drug Master File in Japan (N0837 JDMF) empowers N0837 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 N0837 JDMF during the approval evaluation for pharmaceutical products. At the time of N0837 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 N0837 suppliers with JDMF on PharmaCompass.
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