DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
HEPARIN SODIUM 12,500 UNITS IN DEXTROSE 5%
FDA Application No:
(NDA) 018911
Active Ingredient(s):
HEPARIN SODIUM
Company:
HOSPIRA
Original Approval or Tentative Approval Date:
January 30, 1985
Chemical Type:
5 New manufacturer
Review Classification:
S Standard review drug
Therapeutic Equivalents
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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 Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
HEPARIN SODIUM 10,000 UNITS IN DEXTROSE 5%
HEPARIN SODIUM
10,000 UNITS/100ML
INJECTABLE; INJECTION
Discontinued
No
None
HEPARIN SODIUM 10,000 UNITS IN SODIUM CHLORIDE 0.45%
HEPARIN SODIUM
10,000 UNITS/100ML
INJECTABLE; INJECTION
Discontinued
No
None
HEPARIN SODIUM 10,000 UNITS IN SODIUM CHLORIDE 0.9%
HEPARIN SODIUM
10,000 UNITS/100ML
INJECTABLE; INJECTION
Discontinued
No
None
HEPARIN SODIUM 12,500 UNITS IN DEXTROSE 5%
HEPARIN SODIUM
5,000 UNITS/100ML
INJECTABLE; INJECTION
Discontinued
No
None
HEPARIN SODIUM 12,500 UNITS IN SODIUM CHLORIDE 0.9%
HEPARIN SODIUM
5,000 UNITS/100ML
INJECTABLE; INJECTION
Discontinued
No
None
HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5%
HEPARIN SODIUM
10,000 UNITS/100ML
INJECTABLE; INJECTION
Discontinued
No
None
HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5%
HEPARIN SODIUM
5,000 UNITS/100ML
INJECTABLE; INJECTION
Discontinued
No
None
HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.9%
HEPARIN SODIUM
5,000 UNITS/100ML
INJECTABLE; INJECTION
Discontinued
No
None
HEPARIN SODIUM 5,000 UNITS IN SODIUM CHLORIDE 0.45%
HEPARIN SODIUM
100 UNITS/ML
INJECTABLE; INJECTION
Discontinued
No
None
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