01 1VIRCHOW LABORATORIES LIMITED.
01 1Sulfamethoxazole
01 1India
Registration Number : 302MF10036
Registrant's Address : Plot No. 4 to 10,S. V. Co-operative Indi. Estate,I. D. A. Jeedimetla,Hyderabad-500 05...
Initial Date of Registration : 2020-03-16
Latest Date of Registration : 2020-03-16
A Gantanol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gantanol, including repackagers and relabelers. The FDA regulates Gantanol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gantanol 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 Gantanol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gantanol supplier is an individual or a company that provides Gantanol active pharmaceutical ingredient (API) or Gantanol finished formulations upon request. The Gantanol suppliers may include Gantanol API manufacturers, exporters, distributors and traders.
click here to find a list of Gantanol 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 Gantanol Drug Master File in Japan (Gantanol JDMF) empowers Gantanol 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 Gantanol JDMF during the approval evaluation for pharmaceutical products. At the time of Gantanol 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 Gantanol suppliers with JDMF on PharmaCompass.
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