Visitor Monitoring Drug Details: HEPARIN SODIUM
 
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Drug Details

Drug Name: HEPARIN SODIUM
FDA Application No: (NDA) 017064
Active Ingredient(s): HEPARIN SODIUM
Company: WATSON LABS
Original Approval or Tentative Approval Date: November 22, 1974
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
Therapeutic Equivalents Labels are not available
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
HEPARIN LOCK FLUSH HEPARIN SODIUM100 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 Discontinued No None
HEPARIN SODIUM HEPARIN SODIUM10,000 UNITS/MLINJECTABLE; INJECTION Discontinued No None
HEPARIN SODIUM HEPARIN SODIUM20,000 UNITS/MLINJECTABLE; INJECTION Discontinued No None
HEPARIN SODIUM HEPARIN SODIUM40,000 UNITS/MLINJECTABLE; INJECTION Discontinued No None
HEPARIN SODIUM HEPARIN SODIUM2,500 UNITS/MLINJECTABLE; INJECTION Discontinued No None
HEPARIN SODIUM HEPARIN SODIUM3,000 UNITS/MLINJECTABLE; INJECTION Discontinued No None
HEPARIN SODIUM HEPARIN SODIUM4,000 UNITS/MLINJECTABLE; INJECTION Discontinued No None
HEPARIN SODIUM HEPARIN SODIUM6,000 UNITS/MLINJECTABLE; INJECTION Discontinued No None
HEPARIN SODIUM HEPARIN SODIUM7,500 UNITS/MLINJECTABLE; INJECTION Discontinued No None


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