01 1Abbott Healthcare Products B. V.
02 1Danipharm A/S
03 2Fresenius Kabi iPSUM S. r. l.
01 2Lactulose
02 1Lactulose Crystals
03 1Lactulose Syrup
01 1Denmark
02 1U.S.A
03 2United Kingdom
Registration Number : 219MF10056
Registrant's Address : C. J. van Houtenlaan 36 1381 CP Weesp The Netherlands
Initial Date of Registration : 2007-03-05
Latest Date of Registration : 2024-05-22
Registration Number : 222MF10224
Registrant's Address : Englandsvej 350-356 DK-2770 Kastrup Denmark
Initial Date of Registration : 2010-09-07
Latest Date of Registration : 2010-09-07
Registration Number : 217MF11292
Registrant's Address : Piazza Maestri del Lavoro, 7 20063 Cernusco sul Naviglio (Milano), Italy
Initial Date of Registration : 2005-12-22
Latest Date of Registration : 2014-05-02
Registration Number : 217MF11291
Registrant's Address : via Roma, n. 108 20051 Cassina de'Pecchi (MI), Italy.
Initial Date of Registration : 2005-12-22
Latest Date of Registration : 2014-04-02
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PharmaCompass offers a list of Lactulose 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 Lactulose manufacturer or Lactulose supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lactulose manufacturer or Lactulose supplier.
PharmaCompass also assists you with knowing the Lactulose API Price utilized in the formulation of products. Lactulose API Price is not always fixed or binding as the Lactulose Price is obtained through a variety of data sources. The Lactulose Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Portalac manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Portalac, including repackagers and relabelers. The FDA regulates Portalac manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Portalac 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 Portalac manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Portalac supplier is an individual or a company that provides Portalac active pharmaceutical ingredient (API) or Portalac finished formulations upon request. The Portalac suppliers may include Portalac API manufacturers, exporters, distributors and traders.
click here to find a list of Portalac 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 Portalac Drug Master File in Japan (Portalac JDMF) empowers Portalac 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 Portalac JDMF during the approval evaluation for pharmaceutical products. At the time of Portalac 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 Portalac suppliers with JDMF on PharmaCompass.
We have 3 companies offering Portalac
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