Visitor Monitoring Drug Details: MAXIPIME
 
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Drug Details

Drug Name: MAXIPIME
FDA Application No: (NDA) 050679
Active Ingredient(s): CEFEPIME HYDROCHLORIDE (ARGININE FORMULATION)
Company: BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date: January 18, 1996
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
MAXIPIME CEFEPIME HYDROCHLORIDE (ARGININE FORMULATION)EQ 500MG BASE/VIALINJECTABLE; INJECTION Prescription Yes AP
MAXIPIME CEFEPIME HYDROCHLORIDE (ARGININE FORMULATION)EQ 1GM BASE/VIALINJECTABLE; INJECTION Prescription Yes AP
MAXIPIME CEFEPIME HYDROCHLORIDE (ARGININE FORMULATION)EQ 2GM BASE/VIALINJECTABLE; INJECTION Prescription Yes AP


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