DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
AZATHIOPRINE SODIUM
FDA Application No:
(ANDA) 074419
Active Ingredient(s):
AZATHIOPRINE SODIUM
Company:
BEDFORD
Original Approval or Tentative Approval Date:
March 31, 1995
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
AZATHIOPRINE SODIUM
AZATHIOPRINE SODIUM
EQ 100MG BASE/VIAL
INJECTABLE; INJECTION
Prescription
Yes
None
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