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01 1Cardinal Health
02 1EASTMAN KODAK
03 1Macco Organiques Inc
04 1Merck Group
05 1Niacet b.v
06 1Siemens Molecular Imaging
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01 2SODIUM ACETATE ANHYDROUS
02 1SODIUM ACETATE ANHYDROUS, USP GRADE
03 1SODIUM ACETATE C-11 INJECTION
04 1SODIUM ACETATE C11 INJECTION
05 1a-(2-AMINO-3-p-BROMOBENZOYLPHENYL) ACETIC ACID SODIUM SALT
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01 1Canada
02 2Germany
03 3U.S.A
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01 1Active
02 5Inactive
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01 1Complete
02 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24560
Submission : 2011-01-19
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8132
Submission : 1989-07-13
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2019-11-29
Pay. Date : 2019-10-30
DMF Number : 27844
Submission : 2013-12-20
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31926
Submission : 2017-10-10
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6654
Submission : 1986-10-31
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26352
Submission : 2012-08-24
Status : Inactive
Type : II
59
PharmaCompass offers a list of Sodium Acetate 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 Sodium Acetate manufacturer or Sodium Acetate supplier for your needs.
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A Tox21_202741 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202741, including repackagers and relabelers. The FDA regulates Tox21_202741 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202741 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 Tox21_202741 supplier is an individual or a company that provides Tox21_202741 active pharmaceutical ingredient (API) or Tox21_202741 finished formulations upon request. The Tox21_202741 suppliers may include Tox21_202741 API manufacturers, exporters, distributors and traders.
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A Tox21_202741 DMF (Drug Master File) is a document detailing the whole manufacturing process of Tox21_202741 active pharmaceutical ingredient (API) in detail. Different forms of Tox21_202741 DMFs exist exist since differing nations have different regulations, such as Tox21_202741 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tox21_202741 DMF submitted to regulatory agencies in the US is known as a USDMF. Tox21_202741 USDMF includes data on Tox21_202741's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tox21_202741 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 6 companies offering Tox21_202741
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