Visitor Monitoring Drug Details: ZINACEF
 
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Drug Details

Drug Name: ZINACEF
FDA Application No: (NDA) 050558
Active Ingredient(s): CEFUROXIME SODIUM
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: October 19, 1983
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
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
ZINACEF CEFUROXIME SODIUMEQ 750MG BASE/VIALINJECTABLE; IM-IV Prescription Yes AB
ZINACEF CEFUROXIME SODIUMEQ 1.5GM BASE/VIALINJECTABLE; INJECTION Prescription Yes AP
ZINACEF CEFUROXIME SODIUMEQ 7.5GM BASE/VIALINJECTABLE; INJECTION Prescription Yes AP


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