DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
KINEVAC
FDA Application No:
(NDA) 017697
Active Ingredient(s):
SINCALIDE
Company:
BRACCO
Original Approval or Tentative Approval Date:
July 21, 1976
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
There are no Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
KINEVAC
SINCALIDE
0.005MG/VIAL
INJECTABLE; INJECTION
Prescription
Yes
None
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