DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
URACIL MUSTARD
FDA Application No:
(NDA) 012892
Active Ingredient(s):
URACIL MUSTARD
Company:
SHIRE
Original Approval or Tentative Approval Date:
September 13, 1962
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
There are no 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
URACIL MUSTARD
URACIL MUSTARD
1MG
CAPSULE; ORAL
Discontinued
No
None
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