01 1Bidachem S. p. A
02 1Cambrex Profarmaco Milano S. r. l.
03 1Shreepati Pharmaceuticals Pvt. Ltd.
04 1SperaNexus Co., Ltd.
01 2Pico sulfate sodium
02 1Picosulfate sodium hydrate
03 1Sodium Picosulfate
01 1India
02 1Italy
03 1Japan
04 1U.S.A
Registration Number : 220MF10132
Registrant's Address : S. S. 11 Padana Superiore,N. 8 24040 Fornovo San Giovanni
Initial Date of Registration : 2008-05-20
Latest Date of Registration : 2015-05-01
Registration Number : 217MF11185
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2019-10-08
Registration Number : 217MF10037
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration : 2006-12-18
Registration Number : 305MF10103
Registrant's Address : 208, Silver Arc Plaza, 20/1, New Palasia, Indore, Madhya Paradesh, INDIA
Initial Date of Registration : 2023-08-30
Latest Date of Registration : 2023-08-30
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PharmaCompass offers a list of Sodium Picosulfate 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 Sodium Picosulfate manufacturer or Sodium Picosulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Picosulfate manufacturer or Sodium Picosulfate supplier.
PharmaCompass also assists you with knowing the Sodium Picosulfate API Price utilized in the formulation of products. Sodium Picosulfate API Price is not always fixed or binding as the Sodium Picosulfate Price is obtained through a variety of data sources. The Sodium Picosulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Neopax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neopax, including repackagers and relabelers. The FDA regulates Neopax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neopax 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 Neopax manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Neopax supplier is an individual or a company that provides Neopax active pharmaceutical ingredient (API) or Neopax finished formulations upon request. The Neopax suppliers may include Neopax API manufacturers, exporters, distributors and traders.
click here to find a list of Neopax 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 Neopax Drug Master File in Japan (Neopax JDMF) empowers Neopax 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 Neopax JDMF during the approval evaluation for pharmaceutical products. At the time of Neopax 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 Neopax suppliers with JDMF on PharmaCompass.
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