DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
IMURAN
FDA Application No:
(NDA) 016324
Active Ingredient(s):
AZATHIOPRINE
Company:
PROMETHEUS LABS
Original Approval or Tentative Approval Date:
March 20, 1968
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
IMURAN
AZATHIOPRINE
50MG
TABLET; ORAL
Prescription
Yes
AB
IMURAN
AZATHIOPRINE
25MG
TABLET; ORAL
Discontinued
No
None
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