DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CARDIOGEN-82
FDA Application No:
(NDA) 019414
Active Ingredient(s):
RUBIDIUM CHLORIDE RB-82
Company:
BRACCO
Original Approval or Tentative Approval Date:
December 29, 1989
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard 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
CARDIOGEN-82
RUBIDIUM CHLORIDE RB-82
N/A
INJECTABLE; INJECTION
Prescription
No
None
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