01 1FDC LIMITED.
02 1Sanyo Chemical Research Institute Co., Ltd.
01 1Bromhexine Hydrochloride
02 1Bromhexine hydrochloride
01 1Gabon
02 1India
Registration Number : 305MF10115
Registrant's Address : 142-48,s,v,road,jogeshwari(w),mumbai-400 102 India
Initial Date of Registration : 2023-10-12
Latest Date of Registration : 2023-10-12
Registration Number : 227MF10252
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2015-10-09
Latest Date of Registration : 2023-11-01
22
PharmaCompass offers a list of Bromhexine Hydrochloride 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 Bromhexine Hydrochloride manufacturer or Bromhexine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Bromhexine Hydrochloride API Price utilized in the formulation of products. Bromhexine Hydrochloride API Price is not always fixed or binding as the Bromhexine Hydrochloride Price is obtained through a variety of data sources. The Bromhexine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Flubron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flubron, including repackagers and relabelers. The FDA regulates Flubron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flubron API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Flubron supplier is an individual or a company that provides Flubron active pharmaceutical ingredient (API) or Flubron finished formulations upon request. The Flubron suppliers may include Flubron API manufacturers, exporters, distributors and traders.
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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 Flubron Drug Master File in Japan (Flubron JDMF) empowers Flubron 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 Flubron JDMF during the approval evaluation for pharmaceutical products. At the time of Flubron JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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