DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
RADIONUCLIDE-LABELED (125 I) FIBRINOGEN (HUMAN) SENSOR
FDA Application No:
(NDA) 017787
Active Ingredient(s):
FIBRINOGEN, I-125
Company:
ABBOTT
Original Approval or Tentative Approval Date:
June 28, 1976
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
There are no Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
RADIONUCLIDE-LABELED (125 I) FIBRINOGEN (HUMAN) SENSOR
FIBRINOGEN, I-125
140uCi/ML
INJECTABLE; INJECTION
Discontinued
No
None
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