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
A Scobutyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Scobutyl, including repackagers and relabelers. The FDA regulates Scobutyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Scobutyl 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 Scobutyl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Scobutyl supplier is an individual or a company that provides Scobutyl active pharmaceutical ingredient (API) or Scobutyl finished formulations upon request. The Scobutyl suppliers may include Scobutyl API manufacturers, exporters, distributors and traders.
click here to find a list of Scobutyl 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 Scobutyl Drug Master File in Japan (Scobutyl JDMF) empowers Scobutyl 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 Scobutyl JDMF during the approval evaluation for pharmaceutical products. At the time of Scobutyl 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 Scobutyl suppliers with JDMF on PharmaCompass.
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