Visitor Monitoring Drug Details: ZEMURON
 
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Drug Details

Drug Name: ZEMURON
FDA Application No: (NDA) 020214
Active Ingredient(s): ROCURONIUM BROMIDE
Company: ORGANON USA INC
Original Approval or Tentative Approval Date: March 17, 1994
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard 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
ZEMURON ROCURONIUM BROMIDE50MG/5ML(10MG/ML)INJECTABLE; INJECTION Prescription Yes None
ZEMURON ROCURONIUM BROMIDE10MG/MLINJECTABLE; INJECTION Discontinued No None
ZEMURON ROCURONIUM BROMIDE100MG/10ML(10MG/ML)INJECTABLE; INJECTION Prescription Yes None


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