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
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
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, 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 Laevolac manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Laevolac, including repackagers and relabelers. The FDA regulates Laevolac manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Laevolac 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 Laevolac manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Laevolac supplier is an individual or a company that provides Laevolac active pharmaceutical ingredient (API) or Laevolac finished formulations upon request. The Laevolac suppliers may include Laevolac API manufacturers, exporters, distributors and traders.
click here to find a list of Laevolac suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Laevolac CEP of the European Pharmacopoeia monograph is often referred to as a Laevolac Certificate of Suitability (COS). The purpose of a Laevolac CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Laevolac EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Laevolac to their clients by showing that a Laevolac CEP has been issued for it. The manufacturer submits a Laevolac CEP (COS) as part of the market authorization procedure, and it takes on the role of a Laevolac CEP holder for the record. Additionally, the data presented in the Laevolac CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Laevolac DMF.
A Laevolac CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Laevolac 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 Laevolac suppliers with CEP (COS) on PharmaCompass.
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