Visitor Monitoring Drug Details: ANCEF
 
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Drug Details

Drug Name: ANCEF
FDA Application No: (NDA) 050461
Active Ingredient(s): CEFAZOLIN SODIUM
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: October 4, 1973
 
Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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
ANCEF CEFAZOLIN SODIUMEQ 250MG BASE/VIALINJECTABLE; INJECTION Discontinued No None
ANCEF CEFAZOLIN SODIUMEQ 500MG BASE/VIALINJECTABLE; INJECTION Discontinued No None
ANCEF CEFAZOLIN SODIUMEQ 1GM BASE/VIALINJECTABLE; INJECTION Prescription Yes AP
ANCEF CEFAZOLIN SODIUMEQ 5GM BASE/VIALINJECTABLE; INJECTION Discontinued No None
ANCEF CEFAZOLIN SODIUMEQ 10GM BASE/VIALINJECTABLE; INJECTION Prescription Yes AP


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