01 1Abbott Healthcare Products B. V.
02 1Danipharm A/S
03 2Fresenius Kabi iPSUM S. r. l.
04 1SYNGARS TECHNOLOGY CO. , LTD.
01 3Lactulose
02 1Lactulose Crystals
03 1Lactulose Syrup
01 1Denmark
02 1U.S.A
03 2United Kingdom
04 1Blank
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 : 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 : 2025-12-17
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 : 308MF10043
Registrant's Address : No. 80, Songshan Road, Baishe Country, Lanxi City, Jinhua City, Zhejiang Province, 32...
Initial Date of Registration : 2026-02-19
Latest Date of Registration : 2026-02-19
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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, 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.
A Laxilose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Laxilose, including repackagers and relabelers. The FDA regulates Laxilose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Laxilose 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 Laxilose manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Laxilose supplier is an individual or a company that provides Laxilose active pharmaceutical ingredient (API) or Laxilose finished formulations upon request. The Laxilose suppliers may include Laxilose API manufacturers, exporters, distributors and traders.
click here to find a list of Laxilose suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Laxilose Drug Master File in Japan (Laxilose JDMF) empowers Laxilose 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 Laxilose JDMF during the approval evaluation for pharmaceutical products. At the time of Laxilose 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 Laxilose suppliers with JDMF on PharmaCompass.
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