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01 35N Plus Lubeck GmbH
02 1FIRST RARE MATERIALS CO LTD
03 1Laboratorios Imperiales, S.A. de C.V.
04 1OMICRON QUIMICA SA
05 1Siegfried AG
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01 4BISMUTH SUBSALICYLATE
02 1BISMUTH SUBSALICYLATE PASTE
03 1BISMUTH SUBSALICYLATE SG
04 1BISMUTH SUBSALICYLATE SG FINE
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01 3Canada
02 1China
03 1France
04 1Mexico
05 1Switzerland
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01 5Active
02 2Inactive
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01 7Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16327
Submission : 2002-12-23
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9660
Submission : 1992-04-20
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36384
Submission : 2021-12-15
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27871
Submission : 2013-12-19
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25360
Submission : 2011-10-04
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11889
Submission : 1996-03-11
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 572
Submission : 1963-05-29
Status : Inactive
Type : II
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PharmaCompass offers a list of Bismuth Subsalicylate 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 Bismuth Subsalicylate manufacturer or Bismuth Subsalicylate supplier for your needs.
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A C7H5BiO4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C7H5BiO4, including repackagers and relabelers. The FDA regulates C7H5BiO4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C7H5BiO4 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 C7H5BiO4 supplier is an individual or a company that provides C7H5BiO4 active pharmaceutical ingredient (API) or C7H5BiO4 finished formulations upon request. The C7H5BiO4 suppliers may include C7H5BiO4 API manufacturers, exporters, distributors and traders.
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A C7H5BiO4 DMF (Drug Master File) is a document detailing the whole manufacturing process of C7H5BiO4 active pharmaceutical ingredient (API) in detail. Different forms of C7H5BiO4 DMFs exist exist since differing nations have different regulations, such as C7H5BiO4 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A C7H5BiO4 DMF submitted to regulatory agencies in the US is known as a USDMF. C7H5BiO4 USDMF includes data on C7H5BiO4's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The C7H5BiO4 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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