01 1Mallinckrodt Pharmaceuticals
02 1Merck Serono
03 1Napp Technologies
04 1Syensqo
01 1DIOCTYL ESTERS OF SULFOSUCCINIC ACID (NA, CA, K, SALTS)
02 1DIOCTYL SODIUM SULFOSUCCINATE (45% SOLUTION)
03 1DIOCTYL SODIUM SULFOSUCCINATE 45% IN POLYETHYLENE GYLCOL 400-55%
04 1DIOCYTL SODIUM SULFOSUCCINATE IN POLYETHYLENE GLYSOL 400
01 1Belgium
02 1Germany
03 1Ireland
04 1U.S.A
01 1Active
02 3Inactive
01 4Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3246
Submission : 1978-06-16
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3106
Submission : 1978-01-06
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2972
Submission : 1977-06-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3235
Submission : 1978-06-22
Status : Active
Type : IV
40
PharmaCompass offers a list of Docusate Sodium 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 Docusate Sodium manufacturer or Docusate Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Docusate Sodium API Price utilized in the formulation of products. Docusate Sodium API Price is not always fixed or binding as the Docusate Sodium Price is obtained through a variety of data sources. The Docusate Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Manoxol OT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Manoxol OT, including repackagers and relabelers. The FDA regulates Manoxol OT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Manoxol OT API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Manoxol OT supplier is an individual or a company that provides Manoxol OT active pharmaceutical ingredient (API) or Manoxol OT finished formulations upon request. The Manoxol OT suppliers may include Manoxol OT API manufacturers, exporters, distributors and traders.
click here to find a list of Manoxol OT suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Manoxol OT DMF (Drug Master File) is a document detailing the whole manufacturing process of Manoxol OT active pharmaceutical ingredient (API) in detail. Different forms of Manoxol OT DMFs exist exist since differing nations have different regulations, such as Manoxol OT USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Manoxol OT DMF submitted to regulatory agencies in the US is known as a USDMF. Manoxol OT USDMF includes data on Manoxol OT's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Manoxol OT USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Manoxol OT suppliers with USDMF on PharmaCompass.
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