Visitor Monitoring Drug Details: HEPFLUSH-10
 
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Drug Details

Drug Name: HEPFLUSH-10
FDA Application No: (NDA) 017651
Active Ingredient(s): HEPARIN SODIUM
Company: ABRAXIS PHARM
Original Approval or Tentative Approval Date: February 10, 1978
Chemical Type: 5 New manufacturer
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
HEPARIN LOCK FLUSH HEPARIN SODIUM100 UNITS/MLINJECTABLE; INJECTION Discontinued No None
HEPARIN SODIUM HEPARIN SODIUM10,000 UNITS/MLINJECTABLE; INJECTION Discontinued No None
HEPARIN SODIUM HEPARIN SODIUM1,000 UNITS/MLINJECTABLE; INJECTION Discontinued No None
HEPARIN SODIUM HEPARIN SODIUM5,000 UNITS/MLINJECTABLE; INJECTION Prescription No AP
HEPARIN SODIUM HEPARIN SODIUM20,000 UNITS/MLINJECTABLE; INJECTION Discontinued No None
HEPFLUSH-10 HEPARIN SODIUM10 UNITS/MLINJECTABLE; INJECTION Prescription No AP


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