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 Cefalotin sodium Sterile manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefalotin sodium Sterile, including repackagers and relabelers. The FDA regulates Cefalotin sodium Sterile manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefalotin sodium Sterile 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 Cefalotin sodium Sterile supplier is an individual or a company that provides Cefalotin sodium Sterile active pharmaceutical ingredient (API) or Cefalotin sodium Sterile finished formulations upon request. The Cefalotin sodium Sterile suppliers may include Cefalotin sodium Sterile API manufacturers, exporters, distributors and traders.
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A Cefalotin sodium Sterile DMF (Drug Master File) is a document detailing the whole manufacturing process of Cefalotin sodium Sterile active pharmaceutical ingredient (API) in detail. Different forms of Cefalotin sodium Sterile DMFs exist exist since differing nations have different regulations, such as Cefalotin sodium Sterile USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cefalotin sodium Sterile DMF submitted to regulatory agencies in the US is known as a USDMF. Cefalotin sodium Sterile USDMF includes data on Cefalotin sodium Sterile's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cefalotin sodium Sterile USDMF is kept confidential to protect the manufacturer’s intellectual property.
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