Visitor Monitoring Drug Details: MEFOXIN
 
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Drug Details

Drug Name: MEFOXIN
FDA Application No: (NDA) 050517
Active Ingredient(s): CEFOXITIN SODIUM
Company: MERCK
Original Approval or Tentative Approval Date: October 18, 1978
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
MEFOXIN CEFOXITIN SODIUMEQ 1GM BASE/VIALINJECTABLE; INJECTION Discontinued No None
MEFOXIN CEFOXITIN SODIUMEQ 2GM BASE/VIALINJECTABLE; INJECTION Discontinued No None
MEFOXIN CEFOXITIN SODIUMEQ 10GM BASE/VIALINJECTABLE; INJECTION Discontinued No None


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