01 1Angelini Pharma
02 1Emcure Pharmaceuticals
03 1Ind Swift Laboratories Limited
04 1Micro Labs Limited
05 2Olon S.p.A
06 1Wuhan Wuyao Pharmaceutical
07 1Blank
01 3ACAMPROSATE CALCIUM
02 3ACAMPROSATE CALCIUM USP
03 1ACAMPROSATE CALCIUM, NON-STERILE BULK DRUG SUBSTANCE
04 1HOMOTAURINE (CALCIUM ACAMPROSATE INTERMEDIATE)
01 1China
02 3India
03 3Italy
04 1Blank
01 6Active
02 2Inactive
01 3Complete
02 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21348
Submission : 2008-02-20
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-05-29
Pay. Date : 2014-01-22
DMF Number : 25809
Submission : 2012-03-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-03-07
Pay. Date : 2013-02-15
DMF Number : 21481
Submission : 2008-03-24
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41306
Submission : 2025-02-15
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-04-13
Pay. Date : 2015-09-18
DMF Number : 22625
Submission : 2009-03-13
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21807
Submission : 2008-07-14
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23973
Submission : 2010-08-25
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15819
Submission : 2002-01-23
Status : Inactive
Type : II
Portfolio PDF
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PharmaCompass offers a list of Acamprosate Calcium 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 Acamprosate Calcium manufacturer or Acamprosate Calcium supplier for your needs.
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A AKOS015895192 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AKOS015895192, including repackagers and relabelers. The FDA regulates AKOS015895192 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AKOS015895192 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 AKOS015895192 supplier is an individual or a company that provides AKOS015895192 active pharmaceutical ingredient (API) or AKOS015895192 finished formulations upon request. The AKOS015895192 suppliers may include AKOS015895192 API manufacturers, exporters, distributors and traders.
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A AKOS015895192 DMF (Drug Master File) is a document detailing the whole manufacturing process of AKOS015895192 active pharmaceutical ingredient (API) in detail. Different forms of AKOS015895192 DMFs exist exist since differing nations have different regulations, such as AKOS015895192 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A AKOS015895192 DMF submitted to regulatory agencies in the US is known as a USDMF. AKOS015895192 USDMF includes data on AKOS015895192's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The AKOS015895192 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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