DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
DAYPRO
FDA Application No:
(NDA) 018841
Active Ingredient(s):
OXAPROZIN
Company:
GD SEARLE
Original Approval or Tentative Approval Date:
October 29, 1992
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard 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
DAYPRO
OXAPROZIN
600MG
TABLET; ORAL
Prescription
Yes
AB
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