01 1ABBOTT HEALTHCARE PRODUCTS B.V. Weesp NL
02 1ABBOTT LABORATORIES CO. Victoriaville CA
03 1Danipharm A/S Kastrup DK
04 5Fresenius Kabi Austria GmbH Linz AT
05 1INALCO S.A.S. Milano IT
06 1INALCO SRL Milano IT
07 1Inalco SpA Milano IT
08 1Milei GmbH Stuttgart DE
09 1RELAX LIMITED Luqa MT
01 2Lactulose
02 1Lactulose, liquid
03 1Lactulose, liquid, 620 g/l to 700 g/l
04 1Lactulose, liquid, 63.4% -70.0% w/v
05 1Lactulose, liquid, 634 g/l to 700 g/l
06 1Lactulose, liquid, 660 g/l, 700 g/l
07 1Lactulose, liquid, 667 g/L
08 1Lactulose, liquid, 667g/l
09 1Lactulose, liquid, 670 g/l
10 1Lactulose, liquid, 670g/l, 695g/l, 720g/l
11 1Lactulose, liquid, Process II, 670 g/l
12 1Lactulose, liquid, with sodium benzoate
01 5Austria
02 1Denmark
03 1Germany
04 2India
05 3Italy
06 1Malta
01 1Expired
02 10Valid
03 1Withdrawn by EDQM Failure to CEP procedure
04 1Withdrawn by Holder
Certificate Number : R1-CEP 1997-060 - Rev 04
Status : Valid
Issue Date : 2010-06-10
Type : Chemical
Substance Number : 924
Lactulose, Liquid, 634 G/l To 700 G/l
Certificate Number : R1-CEP 2005-102 - Rev 05
Status : Valid
Issue Date : 2020-02-17
Type : Chemical
Substance Number : 924
Lactulose, Liquid, 620 G/l To 700 G/l
Certificate Number : R1-CEP 2002-162 - Rev 02
Status : Valid
Issue Date : 2013-11-28
Type : Chemical
Substance Number : 924
Certificate Number : R1-CEP 2005-023 - Rev 02
Status : Valid
Issue Date : 2017-09-07
Type : Chemical
Substance Number : 924
Certificate Number : R1-CEP 2002-236 - Rev 03
Status : Valid
Issue Date : 2017-10-11
Type : Chemical
Substance Number : 1230
Lactulose, Liquid, With Sodium Benzoate
Certificate Number : R1-CEP 2015-187 - Rev 00
Status : Valid
Issue Date : 2020-10-30
Type : Chemical
Substance Number : 924
Certificate Number : CEP 2019-138 - Rev 01
Status : Valid
Issue Date : 2024-08-27
Type : Chemical
Substance Number : 924
Certificate Number : R1-CEP 1998-130 - Rev 03
Status : Valid
Issue Date : 2007-11-30
Type : Chemical
Substance Number : 924
Lactulose, Liquid, Process II, 670 G/l
Certificate Number : R0-CEP 2019-324 - Rev 00
Status : Valid
Issue Date : 2020-05-19
Type : Chemical and TSE
Substance Number : 924
Lactulose, Liquid, 660 G/l, 700 G/l
Certificate Number : R1-CEP 1999-168 - Rev 03
Status : Valid
Issue Date : 2014-08-01
Type : Chemical
Substance Number : 924
67
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 Constilac manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Constilac, including repackagers and relabelers. The FDA regulates Constilac manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Constilac 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 Constilac manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Constilac supplier is an individual or a company that provides Constilac active pharmaceutical ingredient (API) or Constilac finished formulations upon request. The Constilac suppliers may include Constilac API manufacturers, exporters, distributors and traders.
click here to find a list of Constilac suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Constilac CEP of the European Pharmacopoeia monograph is often referred to as a Constilac Certificate of Suitability (COS). The purpose of a Constilac CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Constilac EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Constilac to their clients by showing that a Constilac CEP has been issued for it. The manufacturer submits a Constilac CEP (COS) as part of the market authorization procedure, and it takes on the role of a Constilac CEP holder for the record. Additionally, the data presented in the Constilac CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Constilac DMF.
A Constilac CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Constilac CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Constilac suppliers with CEP (COS) on PharmaCompass.
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