01 1SMS LIFE SCIENCES INDIA LIMITED, UNIT-IV
02 1SMS PHARMACEUTICALS LIMITED.
03 1Sogo Pharmaceutical Co., Ltd.
01 2LANOCONAZOLE
02 1Lanoconazole
01 2India
02 1Japan
Registration Number : 226MF10040
Registrant's Address : 1-8-2 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2014-02-19
Latest Date of Registration : 2014-02-19
Registration Number : 221MF10035
Registrant's Address : Plot No. 19-III, Road No. 71, Opp. Bharatiya Vidya Bhavan Public School, Jubilee Hill...
Initial Date of Registration : 2009-02-09
Latest Date of Registration : 2009-02-09
Registration Number : 227MF10073
Registrant's Address : Plot No. 72, H. No.:8-2-334/3&4 Road No. 5, Opp. SBI Executive Enclave, Banjara Hills...
Initial Date of Registration : 2015-03-12
Latest Date of Registration : 2024-02-29
A Lanoconazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lanoconazole, including repackagers and relabelers. The FDA regulates Lanoconazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lanoconazole 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 Lanoconazole manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lanoconazole supplier is an individual or a company that provides Lanoconazole active pharmaceutical ingredient (API) or Lanoconazole finished formulations upon request. The Lanoconazole suppliers may include Lanoconazole API manufacturers, exporters, distributors and traders.
click here to find a list of Lanoconazole 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 Lanoconazole Drug Master File in Japan (Lanoconazole JDMF) empowers Lanoconazole 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 Lanoconazole JDMF during the approval evaluation for pharmaceutical products. At the time of Lanoconazole 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 Lanoconazole suppliers with JDMF on PharmaCompass.
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