Visitor Monitoring Drug Details: HEPARIN SODIUM 25,000 UNITS AND DEXTROSE 5% IN PLASTIC CONTAINER
 
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Drug Details

Drug Name: HEPARIN SODIUM 25,000 UNITS AND DEXTROSE 5% IN PLASTIC CONTAINER
FDA Application No: (NDA) 018814
Active Ingredient(s): HEPARIN SODIUM
Company: BAXTER HLTHCARE
Original Approval or Tentative Approval Date: October 31, 1983
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 SODIUM 10,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER HEPARIN SODIUM2,000 UNITS/100MLINJECTABLE; INJECTION Discontinued No None
HEPARIN SODIUM 20,000 UNITS AND DEXTROSE 5% IN PLASTIC CONTAINER HEPARIN SODIUM4,000 UNITS/100MLINJECTABLE; INJECTION Prescription No AP
HEPARIN SODIUM 25,000 UNITS AND DEXTROSE 5% IN PLASTIC CONTAINER HEPARIN SODIUM5,000 UNITS/100MLINJECTABLE; INJECTION Prescription No AP
HEPARIN SODIUM 25,000 UNITS AND DEXTROSE 5% IN PLASTIC CONTAINER HEPARIN SODIUM10,000 UNITS/100MLINJECTABLE; INJECTION Prescription No AP


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