01 4ACS DOBFAR SPA
02 1Akums Lifesciences
03 1Eli Lilly
01 2CEPHALOTHIN SODIUM
02 1CEPHALOTHIN SODIUM (STERILE) BUFFERED (USP)
03 1CEPHALOTHIN SODIUM, ORAL GRADE
04 2CEPHALOTHIN SODIUM;SODIUM CHLORIDE
01 1India
02 4Italy
03 1U.S.A
01 2Active
02 4Inactive
01 6Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12586
Submission : 1997-07-09
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13546
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13545
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13206
Submission : 1998-04-30
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24679
Submission : 2011-02-25
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13384
Submission : 1998-09-01
Status : Inactive
Type : II
67
PharmaCompass offers a list of Cefalotin sodium Sterile 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 Cefalotin sodium Sterile manufacturer or Cefalotin sodium Sterile supplier for your needs.
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A Cefalotina sodica manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefalotina sodica, including repackagers and relabelers. The FDA regulates Cefalotina sodica manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefalotina sodica 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 Cefalotina sodica supplier is an individual or a company that provides Cefalotina sodica active pharmaceutical ingredient (API) or Cefalotina sodica finished formulations upon request. The Cefalotina sodica suppliers may include Cefalotina sodica API manufacturers, exporters, distributors and traders.
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A Cefalotina sodica DMF (Drug Master File) is a document detailing the whole manufacturing process of Cefalotina sodica active pharmaceutical ingredient (API) in detail. Different forms of Cefalotina sodica DMFs exist exist since differing nations have different regulations, such as Cefalotina sodica USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cefalotina sodica DMF submitted to regulatory agencies in the US is known as a USDMF. Cefalotina sodica USDMF includes data on Cefalotina sodica's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cefalotina sodica USDMF is kept confidential to protect the manufacturer’s intellectual property.
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