DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CYCLOSPORINE
FDA Application No:
(ANDA) 065004
Active Ingredient(s):
CYCLOSPORINE
Company:
BEDFORD
Original Approval or Tentative Approval Date:
October 29, 1999
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
CYCLOSPORINE
CYCLOSPORINE
50MG/ML
INJECTABLE; INJECTION
Prescription
No
AP
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