Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
01 1Alchem International Private Limited
02 1Alps Pharmaceutical Co., Ltd.
01 1Butyl scopolamine bromide
02 1Japanese Pharmacopoeia-butyl scopolamine bromide
01 1India
02 1Japan
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
Registration Number : 229MF10013
Registrant's Address : 201,Empire Plaza,Mehrauli-Gurgaon Road Sultanpur,New Delhi-110 030,INDIA
Initial Date of Registration : 2017-01-23
Latest Date of Registration : 2018-10-26
Japanese Pharmacopoeia Scopolamine Butyl Bromide
Registration Number : 219MF10163
Registrant's Address : 2-10-50 Mukaimachi, Furukawa-cho, Hida-shi, Gifu Prefecture
Initial Date of Registration : 2007-05-21
Latest Date of Registration : 2007-05-21
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PharmaCompass offers a list of Hyoscine Butyl Bromide 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 Hyoscine Butyl Bromide manufacturer or Hyoscine Butyl Bromide supplier for your needs.
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PharmaCompass also assists you with knowing the Hyoscine Butyl Bromide API Price utilized in the formulation of products. Hyoscine Butyl Bromide API Price is not always fixed or binding as the Hyoscine Butyl Bromide Price is obtained through a variety of data sources. The Hyoscine Butyl Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Butylhyoscine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Butylhyoscine, including repackagers and relabelers. The FDA regulates Butylhyoscine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Butylhyoscine 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 Butylhyoscine supplier is an individual or a company that provides Butylhyoscine active pharmaceutical ingredient (API) or Butylhyoscine finished formulations upon request. The Butylhyoscine suppliers may include Butylhyoscine API manufacturers, exporters, distributors and traders.
click here to find a list of Butylhyoscine 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 Butylhyoscine Drug Master File in Japan (Butylhyoscine JDMF) empowers Butylhyoscine 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 Butylhyoscine JDMF during the approval evaluation for pharmaceutical products. At the time of Butylhyoscine 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 Butylhyoscine suppliers with JDMF on PharmaCompass.
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